A gene responsible for Ghosal hemato-diaphyseal dysplasia maps to chromosome 7q33-34

Hum Genet. 2007 Apr;121(2):269-73. doi: 10.1007/s00439-006-0311-1. Epub 2007 Jan 3.

Abstract

Ghosal hemato-diaphyseal dysplasia is a rare autosomal recessive disorder characterized by a progressive sclerosing diaphyseal dysplasia and refractory anemia. The pathogenesis and genetic bases of this syndrome remain hitherto unknown. We have performed a genome wide search in two inbred families originating from Algeria and Tunisia. Here, we report on the mapping of a disease gene to chromosome 7q33-34 (Zmax = 4.21 at theta = 0 at locus D7S2513) in a 3.4 Mb defined by loci D7S2560 and AC091742. Ongoing studies will hopefully lead to identification of the disease-causing gene.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Algeria
  • Camurati-Engelmann Syndrome / genetics*
  • Child, Preschool
  • Chromosome Mapping*
  • Chromosomes, Human, Pair 7*
  • Family Health
  • Female
  • Genetic Predisposition to Disease
  • Genome, Human
  • Humans
  • Infant
  • Male
  • Pedigree
  • Tunisia