Schmitt Gillenwater Kelly syndrome

名词 n.

英文释义

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

词源

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