Schmitt Gillenwater Kelly syndrome

English

Etymology

Named after Edward Schmitt, Jay Y. Gillenwater and Thadeus E. Kelly, who identified it with John M. Opitz in 1962.

Noun

Schmitt Gillenwater Kelly syndrome (uncountable)

  1. A rare autosomal-dominant congenital disorder consisting of radial hypoplasia, triphalangeal thumbs, hypospadias, and maxillary diastema.
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