Third case of cerebral, ocular, dental, auricular, skeletal anomalies (CODAS) syndrome, further delineating a new malformation syndrome: First report of an affected male and review of literature

American Journal of Medical Genetics

Volumn 102, Issue 1, 2001, Pages 44-47

  Micheil Innes, A ^a   Chudley, Albert E ^a   Reed, Martin H ^a   Paul Shuckett, E ^a   Elske Hildes Ripstein, G ^a   Greenberg, Cheryl R ^a,b  

^a UNIVERSITY OF MANITOBA   (Canada)

^b HEALTH SCIENCES CENTRE   (Canada)

Author keywords

Cataracts; Dental anomalies; MCA MR syndromes; Mennonite; Vertebral coronal clefts

Indexed keywords

COLLAGEN;

ARTICLE; BONE MALFORMATION; CANADA; CASE REPORT; CATARACT; CHILD; CODAS SYNDROME; EAR MALFORMATION; FACE DYSMORPHIA; GENE; HUMAN; MALE; MALFORMATION SYNDROME; PHYSICAL EXAMINATION; PRIORITY JOURNAL;

ABNORMALITIES, MULTIPLE; BONE AND BONES; EAR; EYE ABNORMALITIES; HUMANS; INFANT; MALE; SYNDROME; TOOTH ABNORMALITIES;

EID: 0035934014     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/1096-8628(20010722)102:1<44::AID-AJMG1410>3.0.CO;2-7     Document Type: Article

References (5)

1. Epiphyseal, vertebral, and ear (EVE) dysplasia: A new syndrome?
2. CODAS Syndrome: A new distinct MCA/MR syndrome with radiological changes of spondyloepiphyseal dysplasia. Another case report
3. Inherited diseases in North American Mennonites: Focus on Old Colony (Chortitza) Mennonites
4. Newly recognized syndrome of cerebral, ocular, dental, auricular, skeletal anomalies: CODAS syndrome - A case report
5. Use of isolated inbred human populations for identification of disease genes