Linkage study of chronic childhood-onset spinal muscular atrophy (SMA): confirmation of close linkage to D5S39 in French Canadian families

Genomics. 1992 Sep;14(1):188-90. doi: 10.1016/s0888-7543(05)80305-2.

Abstract

Chronic childhood-onset spinal muscular atrophy (SMA) is, after Duchenne muscular dystrophy, the most common neuromuscular disorder in childhood. Recent linkage analyses have mapped this disease to 5q12-5q14. We show that chronic SMA (Types II and III) is tightly linked to the marker locus D5S39 (Zmax = 5.47 at theta = 0.02) in eight French Canadian families. In contrast to previously published results, we do not observe close linkage between chronic SMA and D5S6 (Zmax = 0.34 at theta = 0.18) or D5S78 (Zmax = 0.25 at theta = 0.21). Last, we present a family that appears to be discordant for this localization but may represent the first example of an incompletely penetrant individual.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Canada
  • Chromosomes, Human, Pair 5
  • Chronic Disease
  • Female
  • France / ethnology
  • Genetic Linkage*
  • Genetic Markers
  • Humans
  • Lod Score
  • Male
  • Muscular Atrophy, Spinal / genetics*
  • Pedigree

Substances

  • Genetic Markers