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etiologies-alpha.doc
2005 National Deaf-Blind Child Count
Teaching Research, Monmouth, OR
Primary Etiology
(Alphabetical)
Total 9550
Etiology (Alphabetically), Number of Cases reported
- Aicardi syndrome, 31
- Alport syndrome, 4
- Alstrom syndrome, 22
- Apert syndrome/Acrocephalosyndactyly, Type 1, 10
- Asphyxia, 305
- Bardet-Biedl syndrome (Laurence Moon-Biedl), 10
- Batten disease, 6
- CHARGE association, 563
- Chemically Induced, 25
- Chromosome 18, Ring 18, 25
- Cockayne syndrome, 10
- Cogan Syndrome, 3
- Complication of Prematurity, 1102
- Congenital Rubella, 111
- Congenital Syphilis, 5
- Congenital Toxoplasmosis, 27
- Cornelia de Lange, 77
- Cri du chat syndrome (Chromosome 5p- synd), 14
- Crigler-Najjar syndrome, 1
- Crouzon syndrome (Craniofacial Dysotosis), 18
- Cytomegalovirus (CMV), 331
- Dandy Walker syndrome, 70
- Direct Trauma to the eye and/or ear, 12
- Down syndrome (Trisomy 21 syndrome), 220
- Encephalitis, 92
- Fetal Alcohol syndrome, 47
- Goldenhar syndrome, 78
- Hallgren syndrome, 2
- Hand-Schuller-Christian (Histiocytosis X), 1
- Herpes-Zoster (or Hunt), 1
- Hunter Syndrome (MPS II), 4
- Hurler syndrome (MPS I-H), 12
- Hydrocephaly, 282
- Infections, 32
- Kearns-Sayre syndrome, 5
- Klippel-Feil sequence, 4
- Klippel-Trenaunay-Weber syndrome, 2
- Kniest Dysplasia, 7
- Leber congenital amaurosis, 38
- Leigh Disease, 7
- Maroteaux-Lamy syndrome (MPS VI), 4
- Marshall syndrome, 15
- Maternal Drug Use, 104
- Meningitis, 276
- Microcephaly, 367
- Moebius syndrome, 28
- Monosomy 10p, 1
- Neonatal Herpes Simplex (HSV), 15
- NF1 - Neurofibromatosis (von Recklinghausen dis), 13
- NF2 - Bilateral Acoustic Neurofibromatosis, 6
- No Determination of Etiology, 1574
- Norrie disease, 25
- Optico-Cochleo-Dentate Degeneration, 3
- OTHER: Hereditary Synd/ Disorders, 1174
- OTHER: Post-Natal/ Non-Congenital, 497
- OTHER: Pre-Natal/ Congenital Complications, 584
- Pfieffer syndrome, 16
- Pierre-Robin syndrome, 34
- Prader-Willi, 6
- Refsum syndrome, 27
- Scheie syndrome (MPS I-S), 1
- Severe Head Injury, 211
- Smith-Lemli-Opitz (SLO) syndrome, 6
- Stickler syndrome, 83
- Stroke, 69
- Sturge-Weber syndrome, 6
- Treacher Collins syndrome, 14
- Trisomy 13 (Trisomy 13-15, Patau syndrome), 57
- Trisomy 18 (Edwards syndrome), 30
- Tumors, 70
- Turner syndrome, 13
- UNKNOWN/MISSING, 305
- Usher I syndrome, 177
- Usher II syndrome, 61
- Usher III syndrome, 8
- Vogt-Koyanagi-Harada syndrome, 1
- Waardenburg syndrome, 16
- Wildervanck syndrome, 1
- Wolf-Hirschhorn syndrome (Trisomy 4p), 36
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