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Cephalic disorder

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are mild enough to allow those affected to eventually function independently in society, others are not. Some infants, children, and adults die, others remain totally disabled, and an even larger population is partially disabled, functioning well below normal capacity throughout life.
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cells divide to form new generations of cells; cell migration, the process in which nerve cells move from their place of origin to the place where they will remain for life; cell differentiation, the process during which cells acquire individual characteristics; and
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Damage to the developing nervous system is a major cause of chronic, disabling disorders and, sometimes, death in infants, children, and even adults. The degree to which damage to the developing nervous system harms the mind and body varies enormously. Many
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of the embryo. Four main processes are responsible for the development of the nervous system: cell proliferation, the process in which
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https://web.archive.org/web/20080920160408/http://www.ninds.nih.gov/disorders/cephalic_disorders/detail_cephalic_disorders.htm
105:) join prematurely. Most cephalic disorders are caused by a disturbance that occurs very early in the development of the 361:
https://web.archive.org/web/20051001003618/http://www.ninds.nih.gov/disorders/cephalic_disorders/cephalic_disorders.htm
153:(NINDS) is currently "conducting and supporting research on normal and abnormal brain and nervous system development." 405: 518: 343: 376: 503: 247: 63: 41: 186: 97:. Some cephalic disorders occur when the cranial sutures (the fibrous joints that connect the 30: 458: 454: 277: 35: 73:
Cephalic disorders are not necessarily caused by a single factor, but may be influenced by
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conditions that stem from damage to, or abnormal development of, the budding
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The human nervous system develops from a small, specialized plate of
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The National Institute of Neurological Disorders and Stroke (NINDS)
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taken by the mother, maternal infection, or exposure to
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National Institute of Neurological Disorders and Stroke
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National Institute of Neurological Disorders and Stroke
427: 431: 85:deficiencies, or by environmental exposures during 29: 24: 367:Portions of this article were based on the page: 8: 428: 40: 21: 16:Group of congenital brain or skull defects 137:, a natural process in which cells die. 389: 546:Congenital disorders of nervous system 170:codes are listed below per disorder. 7: 14: 398:"Cephalic Disorders Fact Sheet" 162:More common cephalic disorders 1: 562: 356: 344:Positional plagiocephaly 377:public domain resource 124:to form the brain and 116:on the surface of the 242:Less common cephalies 62: 'head') are 52:Cephalic disorders 533: 532: 187:Holoprosencephaly 49: 48: 25:Cephalic disorder 19:Medical condition 553: 429: 417: 416: 414: 413: 404:. Archived from 394: 359: 278:Craniosynostosis 109:nervous system. 45: 44: 36:Medical genetics 22: 561: 560: 556: 555: 554: 552: 551: 550: 536: 535: 534: 529: 528: 440: 426: 421: 420: 411: 409: 396: 395: 391: 386: 355: 352: 325: 244: 199:Hydranencephaly 164: 159: 39: 20: 17: 12: 11: 5: 559: 557: 549: 548: 538: 537: 531: 530: 527: 526: 515: 496: 461: 441: 436: 435: 433: 432:Classification 425: 424:External links 422: 419: 418: 388: 387: 385: 382: 364: 363: 351: 348: 347: 346: 341: 336: 331: 324: 321: 320: 319: 313: 312: 311: 308:Trigonocephaly 305: 299: 293: 287: 275: 269: 263: 257: 251: 243: 240: 239: 238: 235:Schizencephaly 232: 226: 220: 217:Megalencephaly 214: 208: 202: 196: 190: 184: 178: 163: 160: 158: 155: 68:nervous system 47: 46: 33: 27: 26: 18: 15: 13: 10: 9: 6: 4: 3: 2: 558: 547: 544: 543: 541: 525: 521: 520: 516: 514: 510: 506: 505: 501: 497: 495: 491: 487: 483: 479: 475: 471: 470: 466: 462: 460: 456: 452: 451: 447: 443: 442: 439: 434: 430: 423: 408:on 2008-09-20 407: 403: 399: 393: 390: 383: 381: 380: 378: 374: 370: 362: 358: 354: 353: 349: 345: 342: 340: 339:MOMO syndrome 337: 335: 334:Encephalocele 332: 330: 327: 326: 322: 317: 314: 309: 306: 303: 302:Scaphocephaly 300: 297: 296:Plagiocephaly 294: 291: 288: 285: 284:Brachycephaly 282: 281: 279: 276: 273: 270: 267: 266:Micrencephaly 264: 261: 258: 255: 252: 249: 246: 245: 241: 236: 233: 230: 227: 224: 221: 218: 215: 212: 211:Lissencephaly 209: 206: 203: 200: 197: 194: 191: 188: 185: 182: 179: 176: 173: 172: 171: 169: 161: 156: 154: 152: 147: 144: 138: 136: 131: 127: 123: 119: 115: 110: 108: 104: 100: 96: 92: 88: 84: 80: 76: 71: 69: 65: 61: 57: 53: 43: 37: 34: 32: 28: 23: 517: 498: 463: 444: 410:. Retrieved 406:the original 401: 392: 366: 365: 260:Macrocephaly 229:Porencephaly 223:Microcephaly 205:Iniencephaly 193:Ethmocephaly 181:Colpocephaly 165: 148: 143:disabilities 139: 111: 81:conditions, 72: 59: 51: 50: 316:Polycephaly 254:Exencephaly 175:Anencephaly 126:spinal cord 83:nutritional 412:2008-07-30 384:References 290:Oxycephaly 272:Otocephaly 91:medication 89:, such as 75:hereditary 64:congenital 54:(from 135:apoptosis 122:pregnancy 95:radiation 87:pregnancy 31:Specialty 540:Category 329:Cyclopia 323:See also 280:(Q75.0) 248:Acephaly 524:D009421 371:at the 357:Note 1: 318:(Q89.4) 310:(Q75.0) 304:(Q75.0) 298:(Q67.3) 292:(Q75.0) 286:(Q75.0) 274:(Q18.2) 262:(Q75.3) 256:(Q00.0) 250:(Q00.0) 237:(Q04.6) 231:(Q04.6) 219:(Q04.5) 213:(Q04.3) 207:(Q00.2) 201:(Q04.3) 195:(Q04.2) 189:(Q04.2) 183:(Q04.8) 177:(Q00.0) 101:of the 79:genetic 168:ICD-10 118:embryo 60:κεφαλή 38:  350:Notes 268:(Q02) 225:(Q02) 157:Types 130:nerve 114:cells 107:fetal 103:skull 99:bones 58: 56:Greek 519:MeSH 504:9-CM 459:LA05 455:LA00 166:The 149:The 513:742 509:740 500:ICD 494:Q89 490:Q75 486:Q67 482:Q18 478:Q04 474:Q00 465:ICD 446:ICD 375:'s 77:or 542:: 522:: 507:: 492:, 488:, 484:, 480:, 472:: 469:10 457:, 453:: 450:11 400:. 70:. 511:- 502:- 476:- 467:- 448:- 438:D 415:. 379:.

Index

Specialty
Medical genetics
Edit this on Wikidata
Greek
congenital
nervous system
hereditary
genetic
nutritional
pregnancy
medication
radiation
bones
skull
fetal
cells
embryo
pregnancy
spinal cord
nerve
apoptosis
disabilities
National Institute of Neurological Disorders and Stroke
ICD-10
Anencephaly
Colpocephaly
Holoprosencephaly
Ethmocephaly
Hydranencephaly
Iniencephaly

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