Schmitt Gillenwater Kelly syndrome

短语

释义与例句

n.
  1. 1.

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

    不可数

词源

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

来源：wiktionary