Waardenburg syndrome

Waardenburg syndrome (WS) is a disorder characterized by varying degrees of deafness and minor defects in structures arising from neural crest, including pigmentation anomalies of eyes, hair, and skin. WS is classified into four clinical and genetic phenotypes.

Oligodactyly

A developmental defect resulting in the presence of fewer than the normal number of digits.


Total: 1

                      


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PMID (PMCID)
7573150
MALE Child
Anophthalmos-syndactyly (Waardenburg) syndrome without oligodactyly of toes.
Sayli BS, Akarsu AN, Altan S.
Am J Med Genet. 1995;58(1):18-20.
Anophthalmos-syndactyly (Waardenburg) syndrome without oligodactyly of toes.