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Andersen–Tawil syndrome

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322: 611:, positively charged ions such as sodium and calcium enter the cell through ion channels, depolarising or reversing this polarity. After a contraction has taken place, the cell restores its polarity (or repolarises) by allowing positively charged ions such as potassium to leave the cell, restoring the membrane to its relaxed, polarised state. The genetic mutation found in those with Andersen–Tawil decreases the flow of potassium, slowing the rate of repolarisation which can be seen in individual cardiac muscle cells as a longer action potential and on the surface ECG as a prolonged QT interval. 677:. Clinical diagnostic criteria have been proposed which suggest that a diagnosis can be made if two of the following four criteria are met: (1) periodic paralysis; (2) ventricular arrhythmias (frequent ventricular ectopic beats or ventricular tachycardia), a prolonged QT interval when corrected for rate, and/or a prominent U wave; (3) at least two of the following dysmorphic features: low-set ears, wide-set eyes, a small mandible, fifth-digit clinodactyly, and syndactyly; and (4) a family member with confirmed Andersen–Tawil syndrome. 615: 53: 796: 1269:"2015 ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death: The Task Force for the Management of Patients with Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death of the European Society of Cardiology (ESC)Endorsed by: Association for European Paediatric and Congenital Cardiology (AEPC)" 360: 662: 627:. Early afterdepolarisations, occurring before the cell has fully repolarised, arise due to reactivation of calcium and sodium channels that would normally be inactivated until the next heartbeat is due. Under the right conditions, reactivation of these currents can cause further depolarisation of the cell, facilitated by the 631:. Early afterdepolarisations may occur as single events, but may occur repeatedly leading to multiple rapid activations of the cell. Delayed afterdepolarisations, occurring after repolarisation has completed, arise from the spontaneous release of calcium from the intracellular calcium store known as the 786:
should also be avoided as these can worsen the tendency to periodic paralysis and arrhythmias. Conversely, potassium-containing supplements to increase blood potassium levels may be helpful. Very strenuous or competitive sport should be discouraged as these may increase the risk of arrhythmias,
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gene alter the usual structure and function of potassium channels or prevent the channels from being inserted correctly into the cell membrane. Many mutations prevent a molecule called PIP2 from binding to the channels and effectively regulating their activity. These changes disrupt the flow of
356:. The ventricular tachycardia seen in Andersen–Tawil syndrome often takes a form known as bidirectional ventricular tachycardia. The arrhythmias seen in association with the condition can cause sudden cardiac death, but the risk of this is lower than in other forms of long QT syndrome. 635:. This calcium release then leaves the cell through the sodium calcium exchanger in exchange for sodium, generating a net inward current and depolarising the cell membrane. If this transient inward current is large enough, a premature action potential is triggered. 401:
The third key feature of Andersen–Tawil syndrome is intermittent muscle weakness. This can last from seconds to minutes, but in some cases may last for days at a time. Weakness often occurs at times when the levels of potassium in the blood are lower than normal
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The prolonged action potentials can lead to arrhythmias through several potential mechanisms. The frequent ventricular ectopy and bidirectional VT typical of Andersen–Tawil syndrome are initiated by a triggering beat in the form of an
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As a genetic condition, Andersen–Tawil syndrome cannot be cured. However, many of symptoms of Andersen–Tawil such as blackouts due to abnormal heart rhythms or periodic paralysis can be successfully treated with
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Two types of Andersen–Tawil syndrome have been described, distinguished by the genetic abnormality that is detected. Type 1 Andersen–Tawil, accounting for about 60% of cases, is caused by mutations in the
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affecting several parts of the body. The three predominant features of Andersen–Tawil syndrome include disturbances of the electrical function of the heart characterised by an abnormality seen on an
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can be used to identify the specific mutation in an affected person, which if found can assist with screening family members. Other investigations that may be helpful in making a diagnosis include
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Tawil R, Ptacek LJ, Pavlakis SG, DeVivo DC, Penn AS, Ozdemir C, Griggs RC (March 1994). "Andersen's syndrome: potassium-sensitive periodic paralysis, ventricular ectopy, and dysmorphic features".
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Andersen–Tawil syndrome is very rare, and as of 2013 approximately 200 cases had been described in the medical literature. The condition is estimated to affect one person in every 1,000,000.
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The physical abnormalities associated with Andersen–Tawil syndrome typically affect the head, face, limbs and spine. Abnormalities of the head and face include an unusually small lower jaw (
2903: 2306: 720: 3406: 321: 302:. The condition is very rare and is estimated to affect one person in every million. The three groups of features seen in this condition were first described in 1971 by 588:– the characteristic pattern of voltage changes across the cell membrane that occur with each heart beat, and depolarises the resting membrane potential of cardiac and 3598: 2975: 2951: 2826: 1368:
Andersen ED, Krasilnikoff PA, Overvad H (September 1971). "Intermittent muscular weakness, extrasystoles, and multiple developmental anomalies. A new syndrome?".
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or implantable devices. The rarity of the condition means that many of these treatments are based on consensus opinion as there are too few patients to conduct
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As in other forms of long QT syndrome which predispose those affected to dangerous heart rhythm disturbances, the risk of arrhythmias can be reduced by taking
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The mechanisms underlying the skeletal abnormalities seen in Andersen–Tawil syndrome have not been fully explained. Possibilities include impaired function of
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Mechanisms underlying early afterdepolarisations (EADs) and delayed afterdepolarisations (DADs) responsible for the arrhythmias seen in Andersen–Tawil syndrome
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The muscle weakness seen in those with Andersen–Tawil syndrome arises from the depolarisation of the resting membrane potential caused by a decrease in /
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Donaldson MR, Yoon G, Fu YH, Ptacek LJ (2004). "Andersen-Tawil syndrome: a model of clinical variability, pleiotropy, and genetic heterogeneity".
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Andersen–Tawil syndrome increases the risk of abnormal heart rhythms by disturbing the electrical signals that are used to coordinate individual
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who described the triad of symptoms in 1971, and Rabi Tawil who made significant contributions to the understanding of the condition in 1994.
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The intermittent weakness seen in Andersen–Tawil syndrome also occurs in other forms of periodic paralysis – hypokalaemic periodic paralysis,
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than on the outer side, referred to as their membranes being polarised. The main ion current responsible for maintaining this polarity is /
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as these drugs can promote abnormal heart rhythms. Lists of medications associated with prolongation of the QT interval can be found
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Tristani-Firouzi M, Etheridge SP (2013). "Chapter 32 – Andersen-Tawil and Timothy Syndromes". In Gussak I, Antzelevitch C (eds.).
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to assess for arrhythmias, measurement of blood potassium levels at baseline and during periods of weakness, and measurement of
3570: 3150: 2994: 2205: 1986: 727: 607:, and a decrease in this current leads to less polarity at rest, or a depolarised resting membrane potential. When these cells 719:. The frequent ventricular ectopy and bidirectional ventricular tachycardia seen in Andersen–Tawil syndrome can also occur in 3678: 3632: 3193: 2989: 2840: 2281: 2276: 2200: 315: 250: 2000: 835:– a small device implanted under the skin which can detect dangerous arrhythmias and automatically treat them with a small 3554: 3478: 3381: 3004: 2845: 2783: 2627: 2503: 2432: 2264: 3288: 3179: 2946: 2773: 2622: 2415: 2398: 2331: 2251: 1630: 871:
Although a description of the condition had probably been made by Klein in 1963, Andersen–Tawil syndrome is named after
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potassium ions, leading to the periodic paralysis and abnormal heart rhythms characteristic of Andersen–Tawil syndrome.
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Andersen–Tawil syndrome is generally diagnosed based on symptoms, the findings on examination, and the results of an
386:). Abnormalities of the limbs and spine include an abnormal curvature of the fingers, particularly the fifth finger ( 1309: 1161:
Wit, Andrew L. (2018-06-19). "Afterdepolarizations and triggered activity as a mechanism for clinical arrhythmias".
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Andersen–Tawil Syndrome classically comprises three groups of features: abnormal electrical function of the heart,
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in which a prolonged QT interval is combined with abnormalities in the structure of the heart, in addition to
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Nguyen HL, Pieper GH, Wilders R (December 2013). "Andersen-Tawil syndrome: clinical and molecular aspects".
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may also be helpful. Those at highest risk of recurrent arrhythmias such as those who have already had a
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Priori SG, Blomström-Lundqvist C, Mazzanti A, Blom N, Borggrefe M, Camm J, et al. (November 2015).
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The differential diagnosis for a prolonged QT interval includes other forms of long QT syndrome such as
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in which only the electrical activity of the heart is affected without involving any other organs;
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mutation is not identified. Mutations in a related gene encoding a similar potassium ion channel,
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Statland JM, Fontaine B, Hanna MG, Johnson NE, Kissel JT, Sansone VA, et al. (April 2018).
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of muscle cells and is therefore critical for maintaining the normal functions of skeletal and
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Electrical diseases of the heart. Volume 1, Basic foundations and primary electrical diseases
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Also known as GIRK4, encodes G protein-sensitive inwardly rectifying potassium channels (K
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Andersen–Tawil syndrome is a genetic disorder which in the majority of cases is caused by
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Woosley, Raymond L.; Black, Kristin; Heise, C. William; Romero, Klaus (February 2018).
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Cardiodysrhythmic potassium-sensitive periodic paralysis, long QT syndrome type 7
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Cardiac and skeletal muscle cells, when relaxed, have fewer positively charged
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manner, but may occur due to a new genetic mutation in the affected person.
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Medications should be avoided that further prolong the QT interval such as
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Santana, Luis F.; Cheng, Edward P.; Lederer, W. Jonathan (December 2010).
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Labelled chest X-ray showing an implantable cardioverter defibrillator.
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gene. In type 2 Andersen–Tawil, accounting for about 40% of cases, a
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may sometimes be required. Periodic paralysis can be treated with
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in which a prolonged QT interval is combined with congenital
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Andersen–Tawil syndrome affects the heart by prolonging the
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mutation positive), Type 2 (genetic mutation not identified)
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gene. The condition is often inherited from a parent in an
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catecholaminergic polymorphic ventricular tachycardia
378:), a broad forehead and nasal root, a high arched or 366:– abnormal curvature of 5th finger towards 4th finger 1489: 3662: 3544: 3503: 3396: 3313: 3149: 3140: 3077: 2932: 2923: 2870: 2757: 2748: 2665: 2608: 2517: 2484: 2456: 2414: 2373: 2350: 2324: 2292: 2250: 2231: 2130: 2116: 2016: 1970: 1956: 1872: 1821: 1814: 1751: 1706: 1663: 1654: 1578: 1493: 332:
in a 9-year-old female with Andersen–Tawil syndrome
208: 188: 177: 157: 147: 137: 123: 115: 107: 97: 84: 68: 42: 37: 1477:This article incorporates public domain text from 1046: 1044: 1455:"Andersen's syndrome (Ellen Damgaard Andersen)" 1210: 1208: 787:although gentle exercise should be encouraged. 1092: 1090: 1008: 1006: 1004: 1002: 1000: 998: 996: 994: 992: 990: 988: 986: 984: 982: 901:Veerapandiyan A, Statland JM, Tawil R (2015). 2726: 1631: 980: 978: 976: 974: 972: 970: 968: 966: 964: 962: 896: 894: 892: 890: 888: 847:Periodic paralysis may be improved by taking 523:Encodes inward rectifying potassium current K 8: 1103:Journal of Molecular and Cellular Cardiology 256:Andersen–Tawil syndrome is inherited in an 3146: 2929: 2754: 2733: 2719: 2711: 2247: 2127: 1967: 1948:Arrhythmogenic right ventricular dysplasia 1818: 1660: 1638: 1624: 1616: 1490: 1156: 1154: 1152: 1150: 909:. Seattle (WA): University of Washington. 51: 34: 3638:Progressive symmetric erythrokeratodermia 1336: 1284: 1240: 1130: 260:pattern. It is caused in most cases by a 3652:Clouston's hidrotic ectodermal dysplasia 660: 490: 27:Rare autosomal dominant genetic disorder 1310:"CredibleMeds.org: What does it offer?" 884: 558:3.4) which carry the potassium current 468:) carries a potassium current known as 3599:Keratitis–ichthyosis–deafness syndrome 3418:Congenital absence of the vas deferens 1682:Spontaneous coronary artery dissection 833:implantable cardioverter defibrillator 394:), short stature, and a curved spine ( 183:implantable cardioverter-defibrillator 1479:The U.S. National Library of Medicine 1163:Pacing and Clinical Electrophysiology 475:which is responsible for setting the 374:), low-set ears, widely spaced eyes ( 7: 2006:Nonbacterial thrombotic endocarditis 457:that transports potassium ions into 1015:International Journal of Cardiology 527:2.1 carrying the potassium current 3269:Jervell and Lange-Nielsen syndrome 3208:Jervell and Lange-Nielsen syndrome 2302:Accelerated idioventricular rhythm 1382:10.1111/j.1651-2227.1971.tb06990.x 937:(2nd ed.). London: Springer. 705:Jervell and Lange-Nielsen syndrome 168:Jervell and Lange-Nielsen syndrome 25: 1317:Trends in Cardiovascular Medicine 3679:Nephrogenic diabetes insipidus 2 3067:Congenital insensitivity to pain 3062:Paroxysmal extreme pain disorder 2990:Hypokalemic periodic paralysis 2 2841:Hypokalemic periodic paralysis 1 728:hyperkalaemic periodic paralysis 3571:Hypoplastic left heart syndrome 3382:Thyrotoxic periodic paralysis 2 2995:Hyperkalemic periodic paralysis 2846:Thyrotoxic periodic paralysis 1 1987:Subacute bacterial endocarditis 539:Type 2 Andersen–Tawil syndrome 508:Type 1 Andersen–Tawil syndrome 251:hypokalaemic periodic paralysis 3633:Erythrokeratodermia variabilis 3585:Charcot–Marie–Tooth disease X1 3289:Familial atrial fibrillation 3 3194:Spinocerebellar ataxia type-13 3180:Familial atrial fibrillation 7 2947:Familial hemiplegic migraine 3 2774:Familial hemiplegic migraine 1 584:current. This prolongs of the 483:. Pathogenic mutations in the 316:hypokalemic periodic paralysis 1: 3729:Syndromes affecting the heart 3479:Vitelliform macular dystrophy 3005:Potassium-aggravated myotonia 2784:Spinocerebellar ataxia type-6 2504:Pulseless electrical activity 2433:Multifocal atrial tachycardia 2307:Catecholaminergic polymorphic 1370:Acta Paediatrica Scandinavica 849:carbonic anhydrase inhibitors 296:carbonic anhydrase inhibitors 1027:10.1016/j.ijcard.2013.10.010 3566:Hallermann–Streiff syndrome 3561:Oculodentodigital dysplasia 3126:Pseudohypoaldosteronism 1AR 1115:10.1016/j.yjmcc.2010.09.005 599:on the inner side of their 60:This condition affects the 3750: 2448:Wandering atrial pacemaker 1995:non-infective endocarditis 1936:Endocardial fibroelastosis 811:that block the effects of 651:bone morphogenetic protein 477:resting membrane potential 390:), fused fingers or toes ( 382:, and a long narrow head ( 3689: 2526:hexaxial reference system 2471:Jervell and Lange-Nielsen 2001:Libman–Sacks endocarditis 1329:10.1016/j.tcm.2017.07.010 1065:10.1080/17431380410032490 903:"Andersen-Tawil Syndrome" 685:ambulatory ECG monitoring 292:implantable defibrillator 153:Clinical, genetic testing 59: 50: 2742:Diseases of ion channels 2406:Ventricular fibrillation 1677:Coronary artery aneurysm 717:autism-spectrum disorder 629:sodium-calcium exchanger 586:cardiac action potential 449:The protein made by the 3734:Cardiogenetic disorders 3344:Andersen–Tawil syndrome 2683:Diastolic heart failure 2657:Athletic heart syndrome 2618:Ventricular hypertrophy 2352:Pre-excitation syndrome 2206:Left posterior fascicle 1731:Acute coronary syndrome 1671:Coronary artery disease 1593:Andersen-Tawil syndrome 1286:10.1093/europace/euv319 350:ventricular tachycardia 330:Ventricular Tachycardia 219:Andersen–Tawil syndrome 38:Andersen–Tawil syndrome 18:Andersen-Tawil syndrome 3609:Bart–Pumphrey syndrome 3000:Paramyotonia congenita 2885:Malignant hyperthermia 2201:Left anterior fascicle 1981:infective endocarditis 1766:Hibernating myocardium 1647:Cardiovascular disease 800: 732:paramyotonia congenita 695:Differential diagnosis 670: 633:sarcoplasmic reticulum 619: 367: 342:abnormal heart rhythms 333: 328:showing bidirectional 270:gene which encodes an 243:abnormal heart rhythms 159:Differential diagnosis 91:Abnormal heart rhythms 3534:Mucolipidosis type IV 3079:Constitutively active 2365:Wolff–Parkinson–White 2325:Premature contraction 2223:Adams–Stokes syndrome 1926:Loeffler endocarditis 1736:Myocardial infarction 1425:10.1002/ana.410350313 798: 664: 617: 590:skeletal muscle cells 362: 324: 3465:Osteopetrosis A2, B4 3274:Romano–Ward syndrome 2890:Central core disease 2532:Right axis deviation 2494:Sudden cardiac death 1852:Pericardial effusion 1795:Ventricular aneurysm 831:may benefit from an 817:antiarrhythmic drugs 815:on the heart. Other 701:Romano–Ward syndrome 669:– fusion of two toes 653:signalling cascade. 280:cardiac muscle cells 241:) and a tendency to 164:Romano-Ward syndrome 3019:Long QT syndrome 10 2537:Left axis deviation 2394:Atrial fibrillation 2389:Ventricular flutter 2312:Torsades de pointes 2186:Bundle branch block 2145:Sick sinus syndrome 1931:Cardiac amyloidosis 1916:Tachycardia-induced 1771:Myocardial stunning 1719:Prinzmetal's angina 1688:Coronary thrombosis 1413:Annals of Neurology 784:bendroflumethiazide 625:afterdepolarisation 3714:Cardiac arrhythmia 3614:Vohwinkel syndrome 3604:Ichthyosis hystrix 3493:Bartter syndrome 3 3437:Myotonia congenita 3349:Long QT syndrome 7 3330:Bartter syndrome 2 3284:Long QT syndrome 1 3241:Brugada syndrome 5 3227:Long QT syndrome 6 3213:Long QT syndrome 5 3057:Febrile seizure 3B 3038:Long QT syndrome 3 3033:Brugada syndrome 1 2971:Brugada syndrome 6 2957:Febrile seizure 3A 2860:Brugada syndrome 4 2808:Long QT syndrome 8 2803:Brugada syndrome 3 2640:Atrial enlargement 2438:Pacemaker syndrome 2360:Lown–Ganong–Levine 2282:Junctional ectopic 2277:AV nodal reentrant 1783:Myocardial rupture 1693:Coronary vasospasm 1579:External resources 1459:www.whonamedit.com 1221:Muscle & Nerve 1175:10.1111/pace.13419 1053:Annals of Medicine 843:Periodic paralysis 801: 749:adequately powered 671: 665:Foot with partial 620: 426:autosomal dominant 368: 346:ventricular ectopy 334: 310:Signs and symptoms 258:autosomal dominant 227:long QT syndrome 7 3701: 3700: 3392: 3391: 3354:Short QT syndrome 3279:Short QT syndrome 3255:Short QT syndrome 3166:Episodic ataxia 1 3142:Potassium channel 3136: 3135: 3100:Liddle's syndrome 2919: 2918: 2822:Ocular albinism 2 2779:Episodic ataxia 2 2708: 2707: 2700:Obstructive shock 2604: 2603: 2551:Short QT syndrome 2518:Other / ungrouped 2509:Sinoatrial arrest 2424:Ectopic pacemaker 2320: 2319: 2140:Sinus bradycardia 2112: 2111: 2108: 2107: 1857:Cardiac tamponade 1810: 1809: 1800:Dressler syndrome 1698:Myocardial bridge 1613: 1612: 1233:10.1002/mus.26009 1059:(Suppl 1): 92–7. 944:978-1-4471-4881-4 675:electrocardiogram 569: 568: 326:Electrocardiogram 235:electrocardiogram 223:Andersen syndrome 216: 215: 149:Diagnostic method 32:Medical condition 16:(Redirected from 3741: 3398:Chloride channel 3315:Inward-rectifier 3147: 2930: 2798:Timothy syndrome 2755: 2735: 2728: 2721: 2712: 2673:Cardiac fibrosis 2565:T wave alternans 2458:Long QT syndrome 2252:Supraventricular 2248: 2181:Intraventricular 2128: 1968: 1819: 1664:Coronary disease 1661: 1640: 1633: 1626: 1617: 1491: 1469: 1468: 1466: 1465: 1451: 1445: 1444: 1408: 1402: 1401: 1365: 1359: 1358: 1340: 1314: 1305: 1299: 1298: 1288: 1264: 1255: 1254: 1244: 1212: 1203: 1202: 1158: 1145: 1144: 1134: 1094: 1085: 1084: 1048: 1039: 1038: 1010: 957: 956: 930: 919: 918: 898: 758:General measures 713:Timothy syndrome 689:thyroid function 491: 274:that transports 231:genetic disorder 172:Timothy syndrome 55: 35: 21: 3749: 3748: 3744: 3743: 3742: 3740: 3739: 3738: 3719:Channelopathies 3704: 3703: 3702: 3697: 3685: 3658: 3540: 3499: 3432:Thomsen disease 3413:Cystic fibrosis 3388: 3309: 3132: 3073: 3052:Erythromelalgia 2915: 2866: 2750:Calcium channel 2744: 2739: 2709: 2704: 2695:Rheumatic fever 2661: 2600: 2513: 2480: 2452: 2410: 2369: 2346: 2316: 2288: 2235: 2227: 2121: 2104: 2012: 1961: 1952: 1868: 1862:Hemopericardium 1806: 1747: 1741:Unstable angina 1714:Angina pectoris 1707:Active ischemia 1702: 1650: 1644: 1614: 1609: 1608: 1574: 1573: 1502: 1488: 1473: 1472: 1463: 1461: 1453: 1452: 1448: 1410: 1409: 1405: 1367: 1366: 1362: 1312: 1307: 1306: 1302: 1279:(11): 1601–87. 1266: 1265: 1258: 1214: 1213: 1206: 1160: 1159: 1148: 1096: 1095: 1088: 1050: 1049: 1042: 1012: 1011: 960: 945: 932: 931: 922: 900: 899: 886: 881: 869: 861: 845: 793: 760: 752:clinical trials 740: 697: 681:Genetic testing 659: 641: 606: 583: 574: 564: 557: 533: 526: 474: 412: 312: 247:small lower jaw 33: 28: 23: 22: 15: 12: 11: 5: 3747: 3745: 3737: 3736: 3731: 3726: 3724:Rare syndromes 3721: 3716: 3706: 3705: 3699: 3698: 3690: 3687: 3686: 3684: 3683: 3682: 3681: 3668: 3666: 3660: 3659: 3657: 3656: 3655: 3654: 3642: 3641: 3640: 3635: 3619: 3618: 3617: 3611: 3606: 3601: 3589: 3588: 3587: 3575: 3574: 3573: 3568: 3563: 3550: 3548: 3542: 3541: 3539: 3538: 3537: 3536: 3524: 3523: 3522: 3509: 3507: 3501: 3500: 3498: 3497: 3496: 3495: 3483: 3482: 3481: 3469: 3468: 3467: 3455: 3454: 3453: 3451:Dent's disease 3441: 3440: 3439: 3434: 3422: 3421: 3420: 3415: 3402: 3400: 3394: 3393: 3390: 3389: 3387: 3386: 3385: 3384: 3372: 3371: 3370: 3358: 3357: 3356: 3351: 3346: 3334: 3333: 3332: 3319: 3317: 3311: 3310: 3308: 3307: 3306: 3305: 3293: 3292: 3291: 3286: 3281: 3276: 3271: 3259: 3258: 3257: 3245: 3244: 3243: 3231: 3230: 3229: 3217: 3216: 3215: 3210: 3198: 3197: 3196: 3184: 3183: 3182: 3170: 3169: 3168: 3155: 3153: 3144: 3138: 3137: 3134: 3133: 3131: 3130: 3129: 3128: 3104: 3103: 3102: 3083: 3081: 3075: 3074: 3072: 3071: 3070: 3069: 3064: 3059: 3054: 3042: 3041: 3040: 3035: 3023: 3022: 3021: 3009: 3008: 3007: 3002: 2997: 2992: 2980: 2979: 2978: 2973: 2961: 2960: 2959: 2954: 2949: 2936: 2934: 2927: 2925:Sodium channel 2921: 2920: 2917: 2916: 2914: 2913: 2912: 2911: 2906: 2894: 2893: 2892: 2887: 2874: 2872: 2868: 2867: 2865: 2864: 2863: 2862: 2850: 2849: 2848: 2843: 2831: 2830: 2829: 2824: 2812: 2811: 2810: 2805: 2800: 2788: 2787: 2786: 2781: 2776: 2763: 2761: 2752: 2746: 2745: 2740: 2738: 2737: 2730: 2723: 2715: 2706: 2705: 2703: 2702: 2697: 2692: 2691: 2690: 2688:Cardiac asthma 2685: 2675: 2669: 2667: 2663: 2662: 2660: 2659: 2654: 2653: 2652: 2647: 2637: 2636: 2635: 2630: 2625: 2614: 2612: 2606: 2605: 2602: 2601: 2599: 2598: 2596:Strain pattern 2593: 2592: 2591: 2586: 2581: 2569: 2568: 2567: 2555: 2554: 2553: 2541: 2540: 2539: 2534: 2521: 2519: 2515: 2514: 2512: 2511: 2506: 2501: 2496: 2490: 2488: 2486:Cardiac arrest 2482: 2481: 2479: 2478: 2473: 2468: 2466:Andersen–Tawil 2462: 2460: 2454: 2453: 2451: 2450: 2445: 2440: 2435: 2430: 2420: 2418: 2412: 2411: 2409: 2408: 2403: 2402: 2401: 2391: 2386: 2384:Atrial flutter 2380: 2378: 2371: 2370: 2368: 2367: 2362: 2356: 2354: 2348: 2347: 2345: 2344: 2339: 2334: 2328: 2326: 2322: 2321: 2318: 2317: 2315: 2314: 2309: 2304: 2298: 2296: 2290: 2289: 2287: 2286: 2285: 2284: 2279: 2269: 2268: 2267: 2256: 2254: 2245: 2229: 2228: 2226: 2225: 2220: 2219: 2218: 2213: 2208: 2203: 2198: 2193: 2183: 2178: 2177: 2176: 2171: 2166: 2156: 2147: 2142: 2136: 2134: 2125: 2114: 2113: 2110: 2109: 2106: 2105: 2103: 2102: 2101: 2100: 2095: 2083: 2082: 2081: 2076: 2064: 2063: 2062: 2057: 2045: 2044: 2043: 2038: 2033: 2020: 2018: 2014: 2013: 2011: 2010: 2009: 2008: 2003: 1991: 1990: 1989: 1976: 1974: 1965: 1954: 1953: 1951: 1950: 1945: 1944: 1943: 1938: 1933: 1928: 1923: 1918: 1913: 1908: 1907: 1906: 1894:Cardiomyopathy 1891: 1890: 1889: 1887:Chagas disease 1878: 1876: 1870: 1869: 1867: 1866: 1865: 1864: 1859: 1849: 1848: 1847: 1838: 1827: 1825: 1816: 1812: 1811: 1808: 1807: 1805: 1804: 1803: 1802: 1797: 1787: 1786: 1785: 1775: 1774: 1773: 1768: 1757: 1755: 1749: 1748: 1746: 1745: 1744: 1743: 1738: 1728: 1727: 1726: 1721: 1710: 1708: 1704: 1703: 1701: 1700: 1695: 1690: 1685: 1679: 1674: 1667: 1665: 1658: 1652: 1651: 1645: 1643: 1642: 1635: 1628: 1620: 1611: 1610: 1607: 1606: 1595: 1583: 1582: 1580: 1576: 1575: 1572: 1571: 1560: 1549: 1538: 1519: 1503: 1498: 1497: 1495: 1494:Classification 1487: 1486:External links 1484: 1483: 1482: 1471: 1470: 1446: 1403: 1360: 1300: 1256: 1227:(4): 522–530. 1204: 1169:(8): 883–896. 1146: 1109:(6): 901–903. 1086: 1040: 958: 943: 920: 883: 882: 880: 877: 873:Ellen Andersen 868: 865: 860: 857: 844: 841: 837:electric shock 829:cardiac arrest 792: 789: 759: 756: 739: 736: 696: 693: 658: 655: 639: 604: 581: 573: 570: 567: 566: 562: 555: 552: 545: 540: 536: 535: 531: 524: 521: 514: 509: 505: 504: 501: 498: 495: 481:cardiac muscle 472: 453:gene forms an 411: 408: 311: 308: 304:Ellen Andersen 221:, also called 214: 213: 210: 206: 205: 192: 186: 185: 179: 175: 174: 161: 155: 154: 151: 145: 144: 139: 135: 134: 125: 121: 120: 117: 113: 112: 109: 105: 104: 101: 95: 94: 88: 82: 81: 72: 66: 65: 57: 56: 48: 47: 44: 40: 39: 31: 26: 24: 14: 13: 10: 9: 6: 4: 3: 2: 3746: 3735: 3732: 3730: 3727: 3725: 3722: 3720: 3717: 3715: 3712: 3711: 3709: 3696: 3695: 3688: 3680: 3677: 3676: 3675: 3674: 3670: 3669: 3667: 3665: 3661: 3653: 3650: 3649: 3648: 3647: 3643: 3639: 3636: 3634: 3631: 3630: 3629: 3628: 3624: 3620: 3615: 3612: 3610: 3607: 3605: 3602: 3600: 3597: 3596: 3595: 3594: 3590: 3586: 3583: 3582: 3581: 3580: 3576: 3572: 3569: 3567: 3564: 3562: 3559: 3558: 3557: 3556: 3552: 3551: 3549: 3547: 3543: 3535: 3532: 3531: 3530: 3529: 3525: 3521: 3518: 3517: 3516: 3515: 3511: 3510: 3508: 3506: 3502: 3494: 3491: 3490: 3489: 3488: 3484: 3480: 3477: 3476: 3475: 3474: 3470: 3466: 3463: 3462: 3461: 3460: 3456: 3452: 3449: 3448: 3447: 3446: 3442: 3438: 3435: 3433: 3430: 3429: 3428: 3427: 3423: 3419: 3416: 3414: 3411: 3410: 3409: 3408: 3404: 3403: 3401: 3399: 3395: 3383: 3380: 3379: 3378: 3377: 3373: 3369: 3366: 3365: 3364: 3363: 3359: 3355: 3352: 3350: 3347: 3345: 3342: 3341: 3340: 3339: 3335: 3331: 3328: 3327: 3326: 3325: 3321: 3320: 3318: 3316: 3312: 3304: 3301: 3300: 3299: 3298: 3294: 3290: 3287: 3285: 3282: 3280: 3277: 3275: 3272: 3270: 3267: 3266: 3265: 3264: 3260: 3256: 3253: 3252: 3251: 3250: 3246: 3242: 3239: 3238: 3237: 3236: 3232: 3228: 3225: 3224: 3223: 3222: 3218: 3214: 3211: 3209: 3206: 3205: 3204: 3203: 3199: 3195: 3192: 3191: 3190: 3189: 3185: 3181: 3178: 3177: 3176: 3175: 3171: 3167: 3164: 3163: 3162: 3161: 3157: 3156: 3154: 3152: 3151:Voltage-gated 3148: 3145: 3143: 3139: 3127: 3124: 3123: 3122: 3121: 3116: 3115: 3110: 3109: 3105: 3101: 3098: 3097: 3096: 3095: 3090: 3089: 3085: 3084: 3082: 3080: 3076: 3068: 3065: 3063: 3060: 3058: 3055: 3053: 3050: 3049: 3048: 3047: 3043: 3039: 3036: 3034: 3031: 3030: 3029: 3028: 3024: 3020: 3017: 3016: 3015: 3014: 3010: 3006: 3003: 3001: 2998: 2996: 2993: 2991: 2988: 2987: 2986: 2985: 2981: 2977: 2974: 2972: 2969: 2968: 2967: 2966: 2962: 2958: 2955: 2953: 2950: 2948: 2945: 2944: 2943: 2942: 2938: 2937: 2935: 2933:Voltage-gated 2931: 2928: 2926: 2922: 2910: 2907: 2905: 2902: 2901: 2900: 2899: 2895: 2891: 2888: 2886: 2883: 2882: 2881: 2880: 2876: 2875: 2873: 2869: 2861: 2858: 2857: 2856: 2855: 2851: 2847: 2844: 2842: 2839: 2838: 2837: 2836: 2832: 2828: 2825: 2823: 2820: 2819: 2818: 2817: 2813: 2809: 2806: 2804: 2801: 2799: 2796: 2795: 2794: 2793: 2789: 2785: 2782: 2780: 2777: 2775: 2772: 2771: 2770: 2769: 2765: 2764: 2762: 2760: 2759:Voltage-gated 2756: 2753: 2751: 2747: 2743: 2736: 2731: 2729: 2724: 2722: 2717: 2716: 2713: 2701: 2698: 2696: 2693: 2689: 2686: 2684: 2681: 2680: 2679: 2678:Heart failure 2676: 2674: 2671: 2670: 2668: 2664: 2658: 2655: 2651: 2648: 2646: 2643: 2642: 2641: 2638: 2634: 2631: 2629: 2626: 2624: 2621: 2620: 2619: 2616: 2615: 2613: 2611: 2607: 2597: 2594: 2590: 2589:ST depression 2587: 2585: 2582: 2580: 2577: 2576: 2575: 2574: 2570: 2566: 2563: 2562: 2561: 2560: 2556: 2552: 2549: 2548: 2547: 2546: 2542: 2538: 2535: 2533: 2530: 2529: 2528: 2527: 2523: 2522: 2520: 2516: 2510: 2507: 2505: 2502: 2500: 2497: 2495: 2492: 2491: 2489: 2487: 2483: 2477: 2474: 2472: 2469: 2467: 2464: 2463: 2461: 2459: 2455: 2449: 2446: 2444: 2441: 2439: 2436: 2434: 2431: 2429: 2425: 2422: 2421: 2419: 2417: 2413: 2407: 2404: 2400: 2397: 2396: 2395: 2392: 2390: 2387: 2385: 2382: 2381: 2379: 2377: 2372: 2366: 2363: 2361: 2358: 2357: 2355: 2353: 2349: 2343: 2340: 2338: 2335: 2333: 2330: 2329: 2327: 2323: 2313: 2310: 2308: 2305: 2303: 2300: 2299: 2297: 2295: 2291: 2283: 2280: 2278: 2275: 2274: 2273: 2270: 2266: 2263: 2262: 2261: 2258: 2257: 2255: 2253: 2249: 2246: 2243: 2239: 2234: 2230: 2224: 2221: 2217: 2216:Trifascicular 2214: 2212: 2209: 2207: 2204: 2202: 2199: 2197: 2194: 2192: 2189: 2188: 2187: 2184: 2182: 2179: 2175: 2172: 2170: 2167: 2165: 2162: 2161: 2160: 2157: 2155: 2151: 2148: 2146: 2143: 2141: 2138: 2137: 2135: 2133: 2129: 2126: 2124: 2119: 2115: 2099: 2098:regurgitation 2096: 2094: 2091: 2090: 2089: 2088: 2084: 2080: 2079:regurgitation 2077: 2075: 2072: 2071: 2070: 2069: 2065: 2061: 2060:regurgitation 2058: 2056: 2053: 2052: 2051: 2050: 2046: 2042: 2041:regurgitation 2039: 2037: 2034: 2032: 2029: 2028: 2027: 2026: 2022: 2021: 2019: 2015: 2007: 2004: 2002: 1999: 1998: 1997: 1996: 1992: 1988: 1985: 1984: 1983: 1982: 1978: 1977: 1975: 1973: 1969: 1966: 1964: 1959: 1955: 1949: 1946: 1942: 1939: 1937: 1934: 1932: 1929: 1927: 1924: 1922: 1919: 1917: 1914: 1912: 1909: 1905: 1902: 1901: 1900: 1897: 1896: 1895: 1892: 1888: 1885: 1884: 1883: 1880: 1879: 1877: 1875: 1871: 1863: 1860: 1858: 1855: 1854: 1853: 1850: 1846: 1842: 1839: 1837: 1834: 1833: 1832: 1829: 1828: 1826: 1824: 1820: 1817: 1813: 1801: 1798: 1796: 1793: 1792: 1791: 1788: 1784: 1781: 1780: 1779: 1776: 1772: 1769: 1767: 1764: 1763: 1762: 1759: 1758: 1756: 1754: 1750: 1742: 1739: 1737: 1734: 1733: 1732: 1729: 1725: 1724:Stable angina 1722: 1720: 1717: 1716: 1715: 1712: 1711: 1709: 1705: 1699: 1696: 1694: 1691: 1689: 1686: 1683: 1680: 1678: 1675: 1672: 1669: 1668: 1666: 1662: 1659: 1657: 1653: 1648: 1641: 1636: 1634: 1629: 1627: 1622: 1621: 1618: 1605: 1601: 1600: 1596: 1594: 1590: 1589: 1585: 1584: 1581: 1577: 1570: 1566: 1565: 1561: 1559: 1555: 1554: 1550: 1548: 1544: 1543: 1539: 1537: 1533: 1529: 1528: 1524: 1520: 1518: 1514: 1513: 1509: 1505: 1504: 1501: 1496: 1492: 1485: 1481: 1480: 1475: 1474: 1460: 1456: 1450: 1447: 1442: 1438: 1434: 1430: 1426: 1422: 1419:(3): 326–30. 1418: 1414: 1407: 1404: 1399: 1395: 1391: 1387: 1383: 1379: 1376:(5): 559–64. 1375: 1371: 1364: 1361: 1356: 1352: 1348: 1344: 1339: 1334: 1330: 1326: 1322: 1318: 1311: 1304: 1301: 1296: 1292: 1287: 1282: 1278: 1274: 1270: 1263: 1261: 1257: 1252: 1248: 1243: 1238: 1234: 1230: 1226: 1222: 1218: 1211: 1209: 1205: 1200: 1196: 1192: 1188: 1184: 1180: 1176: 1172: 1168: 1164: 1157: 1155: 1153: 1151: 1147: 1142: 1138: 1133: 1128: 1124: 1120: 1116: 1112: 1108: 1104: 1100: 1093: 1091: 1087: 1082: 1078: 1074: 1070: 1066: 1062: 1058: 1054: 1047: 1045: 1041: 1036: 1032: 1028: 1024: 1020: 1016: 1009: 1007: 1005: 1003: 1001: 999: 997: 995: 993: 991: 989: 987: 985: 983: 981: 979: 977: 975: 973: 971: 969: 967: 965: 963: 959: 954: 950: 946: 940: 936: 929: 927: 925: 921: 916: 912: 908: 904: 897: 895: 893: 891: 889: 885: 878: 876: 874: 866: 864: 858: 856: 854: 853:acetazolamide 850: 842: 840: 838: 834: 830: 826: 822: 818: 814: 810: 806: 805:beta blockers 797: 790: 788: 785: 781: 777: 773: 769: 765: 757: 755: 753: 750: 746: 737: 735: 733: 729: 724: 722: 718: 714: 710: 706: 702: 694: 692: 690: 686: 682: 678: 676: 668: 663: 656: 654: 652: 648: 643: 636: 634: 630: 626: 616: 612: 610: 602: 601:cell membrane 598: 593: 591: 587: 579: 571: 561: 553: 551: 550: 546: 544: 541: 538: 537: 530: 522: 520: 519: 515: 513: 510: 507: 506: 502: 499: 496: 493: 492: 489: 486: 482: 478: 471: 467: 463: 460: 456: 452: 447: 445: 444: 439: 435: 429: 427: 423: 422: 417: 409: 407: 405: 399: 397: 393: 389: 385: 384:scaphocephaly 381: 377: 376:hypertelorism 373: 365: 361: 357: 355: 351: 347: 343: 339: 331: 327: 323: 319: 317: 309: 307: 305: 301: 300:acetazolamide 297: 293: 289: 288:beta-blockers 285: 281: 277: 273: 269: 268: 263: 259: 254: 252: 248: 244: 240: 236: 232: 228: 224: 220: 211: 207: 204: 203:acetazolamide 200: 199:beta-blockers 196: 193: 191: 187: 184: 180: 176: 173: 169: 165: 162: 160: 156: 152: 150: 146: 143: 140: 136: 132: 131: 126: 122: 118: 114: 110: 106: 102: 100: 99:Complications 96: 92: 89: 87: 83: 80: 76: 73: 71: 67: 63: 58: 54: 49: 45: 41: 36: 30: 19: 3694:ion channels 3691: 3671: 3644: 3621: 3591: 3577: 3553: 3526: 3512: 3485: 3471: 3457: 3443: 3424: 3405: 3374: 3360: 3343: 3336: 3322: 3295: 3261: 3247: 3233: 3219: 3200: 3186: 3172: 3158: 3118: 3112: 3106: 3092: 3086: 3044: 3025: 3011: 2982: 2963: 2939: 2896: 2877: 2871:Ligand gated 2852: 2833: 2814: 2790: 2766: 2610:Cardiomegaly 2584:ST elevation 2571: 2557: 2543: 2524: 2465: 2428:Ectopic beat 2376:fibrillation 2211:Bifascicular 2085: 2066: 2047: 2023: 1993: 1979: 1972:Endocarditis 1911:Hypertrophic 1845:Constrictive 1831:Pericarditis 1789: 1777: 1760: 1597: 1586: 1562: 1551: 1540: 1521: 1506: 1476: 1462:. Retrieved 1458: 1449: 1416: 1412: 1406: 1373: 1369: 1363: 1338:10150/627826 1323:(2): 94–99. 1320: 1316: 1303: 1276: 1272: 1224: 1220: 1166: 1162: 1106: 1102: 1056: 1052: 1018: 1014: 934: 906: 870: 862: 859:Epidemiology 846: 802: 761: 741: 725: 698: 679: 672: 644: 637: 621: 594: 575: 559: 547: 528: 516: 484: 469: 450: 448: 441: 437: 433: 430: 419: 413: 404:hypokalaemia 400: 388:clinodactyly 380:cleft palate 372:micrognathia 369: 364:Clinodactyly 354:palpitations 335: 313: 266: 255: 229:, is a rare 226: 222: 218: 217: 181:Medication, 128: 103:Sudden death 29: 3505:TRP channel 2476:Romano–Ward 2443:Parasystole 2342:Ventricular 2294:Ventricular 2233:Tachycardia 2150:Heart block 2132:Bradycardia 1958:Endocardium 1921:Restrictive 1882:Myocarditis 1823:Pericardium 1588:GeneReviews 1021:(1): 1–16. 907:GeneReviews 809:propranolol 791:Arrhythmias 647:osteoclasts 578:heart cells 455:ion channel 338:QT interval 272:ion channel 239:QT interval 212:1:1,000,000 108:Usual onset 62:QT interval 43:Other names 3708:Categories 3692:See also: 2374:Flutter / 2337:Junctional 2272:Junctional 2265:Multifocal 2238:paroxysmal 2154:Sinoatrial 2123:arrhythmia 2118:Conduction 1874:Myocardium 1564:DiseasesDB 1464:2019-09-16 879:References 821:flecainide 813:adrenaline 780:furosemide 768:amiodarone 745:medication 667:syndactyly 572:Mechanisms 392:syndactyly 284:flecainide 195:Flecainide 190:Medication 75:Cardiology 64:(in blue). 2633:Pulmonary 2416:Pacemaker 2087:pulmonary 2068:tricuspid 1904:Alcoholic 1347:1873-2615 1183:1540-8159 1123:1095-8584 953:841465583 825:verapamil 776:diuretics 738:Treatment 657:Diagnosis 416:mutations 396:scoliosis 290:, but an 276:potassium 209:Frequency 178:Treatment 79:Neurology 70:Specialty 3546:Connexin 2499:Asystole 2399:Familial 2093:stenosis 2074:stenosis 2055:stenosis 2036:stenosis 2031:prolapse 1753:Sequelae 1656:Ischemia 1599:Orphanet 1441:22070260 1398:12236896 1355:28801207 1295:26318695 1273:Europace 1251:29125635 1199:49310809 1191:29920724 1141:20850450 1073:15176430 1035:24383070 915:20301441 851:such as 819:such as 807:such as 709:deafness 609:contract 352:causing 344:such as 298:such as 262:mutation 237:(a long 127:Type 1 ( 119:Lifelong 116:Duration 86:Symptoms 2976:GEFS+ 1 2952:GEFS+ 2 2835:CACNA1S 2816:CACNA1F 2792:CACNA1C 2768:CACNA1A 1899:Dilated 1841:Chronic 1649:(heart) 1558:D050030 1433:8080508 1390:4106724 1242:5867231 1132:3623268 1081:7362563 867:History 764:sotalol 418:in the 278:out of 264:in the 142:Genetic 3528:TRPML1 3487:CLCNKB 3376:KCNJ18 3362:KCNJ11 3120:SCNN1G 3114:SCNN1B 3108:SCNN1A 3094:SCNN1G 3088:SCNN1B 2854:CACNB2 2827:CSNB2A 2579:J wave 2332:Atrial 2260:Atrial 2049:aortic 2025:mitral 2017:Valves 1963:valves 1815:Layers 1684:(SCAD) 1547:170390 1536:794.31 1532:426.82 1439:  1431:  1396:  1388:  1353:  1345:  1293:  1249:  1239:  1197:  1189:  1181:  1139:  1129:  1121:  1079:  1071:  1033:  951:  941:  913:  772:online 730:, and 711:; and 563:K(ACh) 543:600734 512:170390 503:Notes 466:Kir2.1 459:muscle 138:Causes 3664:Porin 3520:FSGS2 3514:TRPC6 3473:BEST1 3459:CLCN7 3445:CLCN5 3426:CLCN1 3368:TNDM3 3338:KCNJ2 3324:KCNJ1 3303:BFNS1 3297:KCNQ2 3263:KCNQ1 3249:KCNH2 3235:KCNE3 3221:KCNE2 3202:KCNE1 3188:KCNC3 3174:KCNA5 3160:KCNA1 3046:SCN9A 3027:SCN5A 3013:SCN4B 2984:SCN4A 2965:SCN1B 2941:SCN1A 2909:ARVD2 2904:CPVT1 2666:Other 2650:Right 2628:Right 2242:sinus 2191:Right 1941:Viral 1836:Acute 1790:weeks 1761:hours 1673:(CAD) 1604:37553 1517:I45.8 1437:S2CID 1394:S2CID 1313:(PDF) 1195:S2CID 1077:S2CID 778:like 549:KCNJ5 518:KCNJ2 500:Gene 497:OMIM 494:Type 485:KCNJ2 462:cells 451:KCNJ2 443:KCNJ5 438:KCNJ2 434:KCNJ2 421:KCNJ2 410:Cause 267:KCNJ2 130:KCNJ2 124:Types 111:Birth 3673:AQP2 3646:GJB6 3627:GJB4 3623:GJB3 3593:GJB2 3579:GJB1 3555:GJA1 3407:CFTR 2898:RYR2 2879:RYR1 2645:Left 2623:Left 2240:and 2196:Left 1778:days 1553:MeSH 1542:OMIM 1527:9-CM 1429:PMID 1386:PMID 1351:PMID 1343:ISSN 1291:PMID 1247:PMID 1187:PMID 1179:ISSN 1137:PMID 1119:ISSN 1069:PMID 1031:PMID 949:OCLC 939:ISBN 911:PMID 823:and 782:and 766:and 597:ions 225:and 1569:700 1523:ICD 1508:ICD 1421:doi 1378:doi 1333:hdl 1325:doi 1281:doi 1237:PMC 1229:doi 1171:doi 1127:PMC 1111:doi 1061:doi 1023:doi 1019:170 398:). 348:or 286:or 3710:: 2573:ST 2545:QT 2426:/ 2174:3° 2169:2° 2164:1° 2159:AV 2152:: 1843:/ 1602:: 1591:: 1567:: 1556:: 1545:: 1534:, 1530:: 1515:: 1512:10 1457:. 1435:. 1427:. 1417:35 1415:. 1392:. 1384:. 1374:60 1372:. 1349:. 1341:. 1331:. 1321:28 1319:. 1315:. 1289:. 1277:17 1275:. 1271:. 1259:^ 1245:. 1235:. 1225:57 1223:. 1219:. 1207:^ 1193:. 1185:. 1177:. 1167:41 1165:. 1149:^ 1135:. 1125:. 1117:. 1107:49 1105:. 1101:. 1089:^ 1075:. 1067:. 1057:36 1055:. 1043:^ 1029:. 1017:. 961:^ 947:. 923:^ 887:^ 855:. 839:. 754:. 734:. 723:. 691:. 640:K1 605:K1 592:. 582:K1 565:. 556:ir 534:. 532:K1 525:ir 473:K1 253:. 201:, 197:, 170:, 166:, 77:, 3625:/ 3616:) 3117:/ 3111:/ 3091:/ 2734:e 2727:t 2720:v 2559:T 2244:) 2236:( 2120:/ 1960:/ 1639:e 1632:t 1625:v 1525:- 1510:- 1500:D 1467:. 1443:. 1423:: 1400:. 1380:: 1357:. 1335:: 1327:: 1297:. 1283:: 1253:. 1231:: 1201:. 1173:: 1143:. 1113:: 1083:. 1063:: 1037:. 1025:: 955:. 917:. 560:I 529:I 470:I 402:( 20:)

Index

Andersen-Tawil syndrome

QT interval
Specialty
Cardiology
Neurology
Symptoms
Abnormal heart rhythms
Complications
KCNJ2
Genetic
Diagnostic method
Differential diagnosis
Romano-Ward syndrome
Jervell and Lange-Nielsen syndrome
Timothy syndrome
implantable cardioverter-defibrillator
Medication
Flecainide
beta-blockers
acetazolamide
genetic disorder
electrocardiogram
QT interval
abnormal heart rhythms
small lower jaw
hypokalaemic periodic paralysis
autosomal dominant
mutation
KCNJ2

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