Waardenburg syndrome. A case report and review of literature
Jordan Medical Journal. 2002; 36 (1): 57-59
in English
| IMEMR
| ID: emr-59598
ABSTRACT
Waardenburg syndrome is an autosomal dominantly inherited disorder with variable penetrance affecting 3% of all deaf children[1]. Genetic studies revealed a mutation in the PAX3 geneon the 2Q35 region. The major characteristic features are Dystopia canthorum; Synophrys; Broad nasal root; Depigmentation of hair, skin or both with white forelock; Heterochromic or hypochromic irides and congenital deafness. Genetic heterogenicity has led to classification of affected families as type I with dystopia canthorum, or type II, without dystopia canthorum disease. This article reviews the literature and describes a case of Waardenburg syndrome type I in a twelve month old male child
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Index:
IMEMR (Eastern Mediterranean)
Main subject:
Review
/
Hearing Loss, Sensorineural
/
Genetic Diseases, Inborn
Limits:
Humans
/
Male
Language:
English
Journal:
Jordan Med. J.
Year:
2002
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