Two additional cases of the Ohdo blepharophimosis syndrome

Am J Med Genet. 1993 Nov 1;47(6):901-6. doi: 10.1002/ajmg.1320470618.

Abstract

Two additional cases of the Ohdo blepharophimosis syndrome are described and compared to the 5 patients previously reported. Blepharophimosis, ptosis, dental hypoplasia, mental retardation, and deafness can be considered as common manifestations of the syndrome. Male patients show cryptorchidism and scrotal hypoplasia.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Abnormalities, Multiple / genetics
  • Blepharophimosis / diagnosis*
  • Blepharophimosis / genetics
  • Blepharophimosis / physiopathology
  • Child, Preschool
  • Female
  • Humans
  • Male
  • Syndrome