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A novel locus for brachydactyly type A1 on chromosome 5p13.3-p13.2
  1. C M Armour1,2,
  2. M E McCready2,3,
  3. A Baig2,3,
  4. A G W Hunter1,
  5. D E Bulman2,3,4
  1. 1Eastern Ontario Regional Genetics Programme, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada
  2. 2Ottawa Health Research Institute, and the University of Ottawa Centre for Neuromuscular Disease, Ottawa, Ontario, Canada
  3. 3Department of Biochemistry, Microbiology and Immunology, University of Ottawa, Ottawa, Ontario, Canada
  4. 4Department of Medicine, Division of Neurology, University of Ottawa, Ottawa, Ontario, Canada
  1. Correspondence to:
 Dr D E Bulman, Ottawa Health Research Institute, 501 Smyth Road, Room 4G-101, Ottawa, Ontario, Canada K1H 8L6; 
 dbulman{at}ohri.ca

https://doi.org/10.1136/jmg.39.3.186

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    The brachydactylies are a group of inherited disorders characterised by shortened or malformed digits that are thought to be the result of abnormal growth of the phalanges and/or metacarpals. First classified by Bell into types A, B, C, D, and E, they were reclassified by Temtamy and McKusick1 and Fitch.2 Brachydactyly type A1 (BDA1, MIM 112500) is characterised by shortened or absent middle phalanges. Often the second and fifth digits, as well as the first proximal phalanx, are the most severely affected. In addition, all of the small tubular bones tend to be reduced in size and the metacarpals may be shortened, particularly the fifth metacarpal. Radial/ulnar clinodactyly, as well as malformed or absent epiphyses, have also been reported.1,2 Complex syndromes have been described in which BDA1 is one of a number of manifestations.3

    Recently, genetic linkage for a BDA1 locus has been reported to map to 2q35-q36 in two unrelated Chinese families.4 Subsequent sequence analysis identified mutations in the Indian Hedgehog gene (Ihh) in affected subjects.5 There have been no other reports of linkage for BDA1, although identification of a balanced translocation between 5q11.2 and 17q23 in a girl with Klippel-Feil anomaly and BDA1 suggests that there may be a BDA1 locus on either chromosome 5 or 17. Mastrobattista et al6 examined a number of candidate genes, including HoxD, Msx1, Msx2, FGF1, and FGF2, in two families with BDA1, but did not find evidence of linkage. Genes involved in two of the other types of brachydactyly have been described. Mutations in CDMP1, a member of the TGF-β superfamily, have been found in a variant of autosomal dominant brachydactyly type C in which the middle phalanges of the second, third, and fifth fingers are shortened.7 …

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