Genomic rearrangements in childhood spinal muscular atrophy: linkage disequilibrium with a null allele

J Med Genet. 1995 Feb;32(2):93-6. doi: 10.1136/jmg.32.2.93.

Abstract

Autosomal recessive childhood onset spinal muscular atrophy has been mapped to chromosome 5q13. We report the analysis of a polymorphic microsatellite which shows linkage disequilibrium with the disease. The linkage disequilibrium is observed with a null allele which is seen as the non-inheritance of alleles from one or both parents. The inheritance of a null allele was observed in 26 out of 36 (72%) informative childhood onset spinal muscular atrophy (SMA) families tested, of all types of severity and from a variety of ethnic backgrounds. In seven families segregating for the severe Werdnig-Hoffmann or SMA type I, no alleles were inherited from either parent using this microsatellite. This null allele may represent a deletion which is either closely associated with, or causes, the disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Child
  • Chromosomes, Human, Pair 5 / genetics*
  • DNA Probes
  • DNA, Satellite / genetics
  • Female
  • Finland
  • Gene Deletion
  • Gene Rearrangement / genetics*
  • Genes, Recessive / genetics
  • Humans
  • Linkage Disequilibrium / genetics*
  • Male
  • Muscular Atrophy, Spinal / genetics*
  • Pedigree
  • Polymorphism, Genetic

Substances

  • DNA Probes
  • DNA, Satellite