Heterozygous deletion at 14q22.1-q22.3 including the BMP4 gene in a patient with psychomotor retardation, congenital corneal opacity and feet polysyndactyly

Am J Med Genet A. 2008 Nov 15;146A(22):2905-10. doi: 10.1002/ajmg.a.32519.

Abstract

Here we report on a 1-year-old Japanese girl with psychomotor retardation, bilateral congenital corneal opacity and bilateral postaxial polysyndactyly of the feet. Although she had a normal female karyotype, our in-house bacterial artificial chromosome (BAC)-based array-CGH analysis successfully detected at least a 2.7-Mb heterozygous deletion at 14q22.1-q22.3 harboring 18 protein-coding genes. Among the genes, BMP4 was a candidate for the gene causing the abnormalities of both the eye and digits. It was previously reported that the BMP family was correlated with the morphogenesis of digits and ocular development, and Bmp4 heterozygous null mice revealed skeletal abnormalities including polydactyly and ocular anterior segment abnormalities. Patients with a deletion including BMP4 also hadabnormalities of the eye and digits. These previous reports support that a haplo-insufficiency of the BMP4 gene likely caused the congenital ocular and digit abnormalities. Moreover, among the other genes contained in the deletion, GMFB is a candidate for the gene responsible for the psychomotor retardation.

Publication types

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

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Bone Morphogenetic Protein 4 / genetics*
  • Cataract / congenital
  • Cataract / genetics
  • Chromosome Deletion*
  • Chromosomes, Artificial, Bacterial / genetics
  • Chromosomes, Human, Pair 14 / genetics*
  • Comparative Genomic Hybridization
  • Female
  • Heterozygote
  • Humans
  • In Situ Hybridization, Fluorescence
  • Infant
  • Psychomotor Disorders / genetics
  • Syndactyly / genetics
  • Toes / abnormalities

Substances

  • BMP4 protein, human
  • Bone Morphogenetic Protein 4