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A third novel locus for primary autosomal recessive microcephaly maps to chromosome 9q34.

Primary autosomal recessive microcephaly is a clinical diagnosis of exclusion in an individual with a head circumference >/=4 SDs below the expected age-and-sex mean. There is associated moderate mental retardation, and neuroimaging shows a small but structurally normal cerebral cortex. The inheritance pattern in the majority of cases is considered to be autosomal recessive. Although genetic heterogeneity for this clinical phenotype had been expected, this has only recently been demonstrated, with the mapping of two loci for autosomal recessive primary microcephaly: MCPH1 at 8p and MCPH2 at 19q. We have studied a large multiaffected consanguineous pedigree, using a whole-genome search, and have identified a third locus, MCPH3 at 9q34. The minimal critical region is approximately 12 cM, being defined by the markers cen-D9S1872-D9S159-tel, with a maximum two-point LOD score of 3.76 (recombination fraction 0) observed for the marker D9S290.

Pubmed ID: 10677332

Authors

  • Moynihan L
  • Jackson AP
  • Roberts E
  • Karbani G
  • Lewis I
  • Corry P
  • Turner G
  • Mueller RF
  • Lench NJ
  • Woods CG

Journal

American journal of human genetics

Publication Data

February 30, 2000

Associated Grants

None

Mesh Terms

  • Chromosome Mapping
  • Chromosomes, Human, Pair 9
  • Consanguinity
  • Female
  • Genes, Recessive
  • Genetic Heterogeneity
  • Humans
  • Lod Score
  • Male
  • Microcephaly
  • Pedigree