Radial hypoplasia-triphalangeal thumbs-hypospadias-maxillary diastema syndrome

A syndrome is characterized by symmetric, nonopposable triphalangeal thumbs and radial hypoplasia. It has been described in eight patients (five females and three males) spanning generations of a family. The affected males also presented with hypospadias. The syndrome is inherited as an autosomal dominant trait.

Also known as: Schmitt Gillenwater Kelly syndrome, Schmitt-Gillenwater-Kelly syndrome, radial hypoplasia triphalangeal thumbs hypospadias maxillary diastema, radial hypoplasia, triphalangeal thumbs, hypospadias, and maxillary diastema, radial hypoplasia, triphalangeal thumbs and hypospadias

0 clinical trials for this condition and its sub-types, 0 tagged with Radial hypoplasia-triphalangeal thumbs-hypospadias-maxillary diastema syndrome itself.