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[Waardenburg's syndrome].

Comptes rendus des seances de la Societe de biologie et de ses filiales - 1 Jan 1996

Cacheux V, Delezoide A L, Vekemans M

Abstract excerpt

Waardenburg syndrome is an autosomal dominant disorder characterised by sensorineural hearing loss, pigmentary abnormalities of iris, hair and skin and dystopia canthorum. The expression of clinical findings of Waardenburg syndrome is extremely variable. The potential sources of this variability include allelic variation, genetic heterogeneity, epistatic modifying genes and stochastic effects. This type of...

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PMID: 9074723

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Source receipt: pubmed, retrieved 7 Sept 2026.

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