Grompe M, Rao N, Elder F F, Caskey C T, Greenberg F
Institute for Molecular Genetics, Baylor College of Medicine, Houston, Tex 77030.
Am J Med Genet. 1992 Jan 1;42(1):39-43. doi: 10.1002/ajmg.1320420110.
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.