45,X/46,X,+r(X) can have a distinct phenotype different from Ullrich-Turner syndrome

Am J Med Genet. 1992 Jan 1;42(1):39-43. doi: 10.1002/ajmg.1320420110.

Abstract

We present a patient with 45,X/46,X,+r(X) mosaicism and lack of inactivation of either the normal or the ring X in the 46,X,+r(X) cells. The patient has mental retardation, syndactyly, minor facial anomalies, and a congenital heart defect. Although most patients with 45,X/46,X,+r(X) have the Ullrich-Turner syndrome, 2 previously described patients with this karyotype also had a distinct phenotype consisting of severe mental retardation, syndactyly, and abnormal face. The unusually severe phenotype in these patients was thought to be due to lack of X-inactivation of the ring X chromosome. The findings in our patient support this hypothesis.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Child, Preschool
  • Dosage Compensation, Genetic
  • Face / abnormalities
  • Female
  • Heart Defects, Congenital / genetics
  • Humans
  • Intellectual Disability / genetics
  • Male
  • Mosaicism*
  • Pedigree
  • Phenotype
  • Ring Chromosomes*
  • Syndactyly / genetics
  • Turner Syndrome / genetics*
  • X Chromosome*