Primary autosomal recessive microcephaly (MCPH1) maps to chromosome 8p22-pter

Am J Hum Genet. 1998 Aug;63(2):541-6. doi: 10.1086/301966.

Abstract

Primary (or "true") microcephaly is inherited as an autosomal recessive trait and is thought to be genetically heterogeneous. Using autozygosity mapping, we have identified a genetic locus (MCPH1) for primary microcephaly, at chromosome 8p22-pter, in two consanguineous families of Pakistani origin. Our results indicate that the gene lies within a 13-cM region between the markers D8S1824 and D8S1825 (maximum multipoint LOD score of 8.1 at D8S277). In addition, we have demonstrated the genetic heterogeneity of this condition by analyzing a total of nine consanguineous families with primary microcephaly.

Publication types

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

MeSH terms

  • Chromosome Mapping
  • Chromosomes, Human, Pair 8*
  • Consanguinity
  • Family
  • Female
  • Genes, Recessive*
  • Genetic Markers
  • Humans
  • Male
  • Microcephaly / genetics*
  • Microsatellite Repeats
  • Pakistan / ethnology
  • Probability
  • United Kingdom

Substances

  • Genetic Markers