Knowledge (XXG)

Familial renal amyloidosis

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Uemichi T, Liepnieks JJ, Gertz MA, Benson MD (September 1998). "Fibrinogen A alpha chain Leu 554: an African-American kindred with late onset renal amyloidosis".
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Gillmore JD, Lachmann HJ, Rowczenio D, Gilbertson JA, Zeng CH, Liu ZH, Li LS, Wechalekar A, Hawkins PN (2009).
1327: 1268: 981: 815: 77: 456:"Hereditary renal amyloidosis caused by a heterozygous G654A gelsolin mutation: a report of two cases" 128:"Diagnosis, pathogenesis, treatment, and prognosis of hereditary fibrinogen A alpha-chain amyloidosis" 1484: 1335: 1248: 1244: 1082: 1035: 679: 628: 223: 1295: 684: 546: 454:
Yamanaka, S.; Miyazaki, Y.; Kasai, K.; Ikeda, S.-i.; Kiuru-Enari, S.; Hosoya, T. (March 27, 2013).
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Li, Danyang; Liu, Dan; Xu, Hui; Yu, Xiao-juan; Zhou, Fu-de; Zhao, Ming-hui; Wang, Su-xia (2019).
341: 403:"Typing of hereditary renal amyloidosis presenting with isolated glomerular amyloid deposition" 95:
It is also known as "Ostertag" type, after B. Ostertag, who characterized it in 1932 and 1950.
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Ostertag B. (1932). "Demonstration einer eigenartigen familiaren paraamyloidose".
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It is associated most commonly with congenital mutations in the
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Granel B, Valleix S, Serratrice J, et al. (January 2006).
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Soutar AK, Hawkins PN, Vigushin DM, et al. (August 1992).
620: 271:"Underdiagnosed amyloidosis: amyloidosis of lysozyme variant" 269:
Granel B, Serratrice J, Disdier P, et al. (March 2005).
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Familial visceral amyloidosis, hereditary amyloid nephropathy
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This condition is inherited in an autosomal dominant manner
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Ostertag, B. (1950). "Familiaere Amyloid-erkrankung".
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Oxford University Press (OUP): 189–193. 132:Journal of the American Society of Nephrology 8: 80:and classified as a dysfibrinogenemia (see 1461: 1447: 1300: 1259:Familial apoprotein CII deficiency/Type Ib 1212: 1198: 1190: 1066: 969: 946: 932: 924: 779: 643: 629: 621: 510: 82:Hereditary Fibrinogen Aα-Chain Amyloidosis 35: 18: 487: 436: 418: 327: 286: 245: 235: 151: 1274:Familial dysbetalipoproteinemia/Type III 1020:Membranoproliferative/mesangiocapillary 104: 1264:Familial hypercholesterolemia/Type IIa 1279:Familial hypertriglyceridemia/Type IV 1254:Lipoprotein lipase deficiency/Type Ia 811:ACys+ABri/Cerebral amyloid angiopathy 765:ATTR/Transthyretin-related hereditary 7: 1415: 1413: 1433:. You can help Knowledge (XXG) by 380:Z. Menschl. Vererb. Konstitutionsl 14: 329:10.1097/01.md.0000200467.51816.6d 1417: 1399:APOA1 familial renal amyloidosis 1269:Combined hyperlipidemia/Type IIb 1144:Granulomatosis with polyangiitis 955:Disease of the kidney glomerules 834:AApoA1+AFib+ALys/Familial renal 760:AA/Familial Mediterranean fever 1: 1346:Chylomicron retention disease 880:ACal/Medullary thyroid cancer 852:Primary cutaneous amyloidosis 750:Aβ2M/Haemodialysis-associated 1305:Hypoalphalipoproteinemia/HDL 288:10.1016/j.amjmed.2004.10.022 216:Proc. Natl. Acad. Sci. U.S.A 69:primarily presenting in the 1341:Apolipoprotein B deficiency 1328:Hypobetalipoproteinemia/LDL 1015:Endocapillary proliferative 806:Familial amyloid neuropathy 1506: 1412: 63:Familial renal amyloidosis 22:Familial renal amyloidosis 1368:Barraquer–Simons syndrome 1097:Type III hypersensitivity 775:Organ-limited amyloidosis 420:10.1186/s12882-019-1667-5 189:10.3109/13506129809003844 43: 34: 1149:Microscopic polyangiitis 1075:Type II hypersensitivity 1010:Mesangial proliferative 460:Clinical Kidney Journal 237:10.1073/pnas.89.16.7389 1490:Genetic disorder stubs 1286:Xanthoma/Xanthomatosis 816:Aβ/Alzheimer's disease 144:10.1681/ASN.2008060614 78:fibrinogen alpha chain 1115:diffuse proliferative 1336:Abetalipoproteinemia 1249:Hypertriglyceridemia 1245:Hypercholesterolemia 1083:Goodpasture syndrome 790:AANF/Isolated atrial 733:Systemic amyloidosis 361:Zentralbl Aug Pathol 316:Medicine (Baltimore) 1480:Glomerular diseases 1296:Hypolipoproteinemia 228:1992PNAS...89.7389S 1394:Lipoid proteinosis 1179:glomerulonephrosis 1174:glomerulonephritis 1105:Post-streptococcal 595:External resources 472:10.1093/ckj/sft007 1442: 1441: 1407: 1406: 1389:Adiposis dolorosa 1354: 1353: 1187: 1186: 1162: 1161: 1049: 1048: 974:Non-proliferative 921: 920: 917: 916: 892:APro/Prolactinoma 755:AGel/Finnish type 618: 617: 86:apolipoprotein A1 60: 59: 16:Medical condition 1497: 1463: 1456: 1449: 1427:genetic disorder 1421: 1414: 1301: 1225:lipid metabolism 1214: 1207: 1200: 1191: 1067: 970: 948: 941: 934: 925: 904:AIAPP/Insulinoma 780: 663:forming proteins 645: 638: 631: 622: 511: 501: 491: 450: 440: 422: 388: 387: 375: 369: 368: 356: 350: 349: 331: 307: 301: 300: 290: 266: 260: 259: 249: 239: 207: 201: 200: 172: 166: 165: 155: 123: 117: 116: 109: 39: 19: 1505: 1504: 1500: 1499: 1498: 1496: 1495: 1494: 1470: 1469: 1468: 1467: 1410: 1408: 1403: 1372: 1350: 1322: 1318:Tangier disease 1290: 1231: 1218: 1188: 1183: 1158: 1126: 1087: 1060: 1055: 1045: 1024: 996: 987:Focal segmental 963: 957: 952: 922: 913: 909:Type 2 diabetes 861: 857:Amyloid purpura 838: 820: 792: 769: 728: 654: 649: 619: 614: 613: 590: 589: 522: 508: 453: 400: 397: 395:Further reading 392: 391: 377: 376: 372: 358: 357: 353: 309: 308: 304: 268: 267: 263: 222:(16): 7389–93. 209: 208: 204: 174: 173: 169: 125: 124: 120: 111: 110: 106: 101: 17: 12: 11: 5: 1503: 1501: 1493: 1492: 1487: 1482: 1472: 1471: 1466: 1465: 1458: 1451: 1443: 1440: 1439: 1422: 1405: 1404: 1402: 1401: 1396: 1391: 1386: 1380: 1378: 1374: 1373: 1371: 1370: 1364: 1362: 1356: 1355: 1352: 1351: 1349: 1348: 1343: 1338: 1332: 1330: 1324: 1323: 1321: 1320: 1315: 1309: 1307: 1298: 1292: 1291: 1289: 1288: 1283: 1282: 1281: 1276: 1271: 1266: 1261: 1256: 1241: 1239: 1237:Hyperlipidemia 1233: 1232: 1219: 1217: 1216: 1209: 1202: 1194: 1185: 1184: 1182: 1181: 1176: 1170: 1168: 1164: 1163: 1160: 1159: 1157: 1156: 1151: 1146: 1140: 1138: 1128: 1127: 1125: 1124: 1119: 1118: 1117: 1107: 1101: 1099: 1089: 1088: 1086: 1085: 1079: 1077: 1064: 1051: 1050: 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J. Med 99:References 55:Nephrology 1057:nephritic 1054:Primarily 965:nephrotic 962:Primarily 887:Pituitary 867:Endocrine 604:eMedicine 480:2048-8505 429:1471-2369 113:"Amyloid" 50:Specialty 1036:Diabetic 899:Pancreas 609:med/3379 498:26019848 447:31870425 367:: 253–4. 338:16523055 297:15745733 162:19073821 90:lysozyme 1167:General 875:Thyroid 661:amyloid 659:Common 574:C538249 489:4432447 438:6929319 346:9761588 256:1502149 224:Bibcode 197:9818055 177:Amyloid 153:2637055 826:Kidney 563:105200 496:  486:  478:  445:  435:  427:  344:  336:  295:  254:  244:  195:  160:  150:  71:kidney 1425:This 1377:Other 1110:Lupus 798:Brain 784:Heart 699:AIAPP 585:33335 552:277.3 537:E85.0 342:S2CID 247:49715 1431:stub 1223:of 844:Skin 724:ABri 719:ACys 714:AANF 709:APro 704:ACal 680:Aβ2M 675:ATTR 569:MeSH 558:OMIM 547:9-CM 494:PMID 476:ISSN 443:PMID 425:ISSN 334:PMID 293:PMID 252:PMID 193:PMID 158:PMID 88:and 1122:IgA 1062:RPG 694:APP 543:ICD 528:ICD 484:PMC 468:doi 433:PMC 415:doi 324:doi 283:doi 279:118 242:PMC 232:doi 185:doi 148:PMC 140:doi 1476:: 1227:: 690:Aβ 685:AL 670:AA 607:: 583:: 572:: 561:: 550:: 535:: 532:10 492:. 482:. 474:. 462:. 458:. 441:. 431:. 423:. 411:20 409:. 405:. 384:30 382:. 365:56 363:. 340:. 332:. 320:85 318:. 314:. 291:. 277:. 273:. 250:. 240:. 230:. 220:89 218:. 214:. 191:. 179:. 156:. 146:. 136:20 134:. 130:. 92:. 73:. 1462:e 1455:t 1448:v 1437:. 1247:/ 1213:e 1206:t 1199:v 1134:/ 1095:/ 1073:/ 1059:, 947:e 940:t 933:v 692:/ 644:e 637:t 630:v 545:- 530:- 520:D 500:. 470:: 464:6 449:. 417:: 348:. 326:: 299:. 285:: 258:. 234:: 226:: 199:. 187:: 181:5 164:. 142:: 115:.

Index


Specialty
Nephrology
amyloidosis
kidney
fibrinogen alpha chain
Hereditary Fibrinogen Aα-Chain Amyloidosis
apolipoprotein A1
lysozyme
"Amyloid"
"Diagnosis, pathogenesis, treatment, and prognosis of hereditary fibrinogen A alpha-chain amyloidosis"
doi
10.1681/ASN.2008060614
PMC
2637055
PMID
19073821
doi
10.3109/13506129809003844
PMID
9818055
"Apolipoprotein AI mutation Arg-60 causes autosomal dominant amyloidosis"
Bibcode
1992PNAS...89.7389S
doi
10.1073/pnas.89.16.7389
PMC
49715
PMID
1502149

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