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Article

Analysis of variability of clinical manifestations in Waardenburg syndrome.

American journal of medical genetics - 17 Jul 1995

Reynolds J E, Meyer J M, Landa B, Stevens C A, Arnos K S, Israel J, Marazita M L, Bodurtha J, Nance W E, Diehl S R

Abstract excerpt

Expression of clinical findings of Waardenburg syndrome type 1 (WS1) and type 2 (WS2) is extremely variable. Using our collection of 26 WS1 and 8 WS2 families, we analyzed the occurrence, severity, and symmetry of clinical manifestations associated with WS. We found significant differences between WS1 and WS2 in deafness, and in pigmentary and craniofacial anomalies. Factor analysis was used to identify...

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Identifiers

PMID: 7573125
DOI: 10.1002/ajmg.1320570405

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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