Confirmation of genetic homogeneity of syndactyly type 1 in an Iranian family

Mohsen Ghadami, Keyvan Majidzadeh-A, Batool Sadat Haerian, Elia Damavandi, Koki Yamada, Parvin Pasallar, Mohammad Taghi Najafi, Gen Nishimura, Hiro Aki Tomita, Koh Ichiro Yoshiura, Norio Niikawa

Research output: Contribution to journalArticlepeer-review

14 Citations (Scopus)


Syndactyly type 1 (SD1) is the most common type of syndactyly, inherited in an autosomal dominant fashion and characterized by complete or partial webbings between the third and fourth fingers and/or between the second and third toes. We recently encountered an Iranian family in which 33 members in six generations were affected with SD1. As a locus of SD1 in a German family has recently been assigned to chromosome 2q34-q36, we performed a linkage analysis of the Iranian SD1 in order to know whether the disorder is genetically homogeneous. With the analysis on 15 affected and 16 unaffected persons in the Iranian family, using dinucleotide repeat polymorphisms as markers, we mapped the SD1 locus to 2q34-q36 with a maximum LOD score of 6.92 at a recombination fraction θ = 0.00 (penetrance = 1.00) for the D2S2179 locus. The result not only confirmed the gene assignment, but also suggests genetic homogeneity of the disease.

Original languageEnglish
Pages (from-to)147-151
Number of pages5
JournalAmerican journal of medical genetics
Issue number2
Publication statusPublished - 2001 Nov 22
Externally publishedYes


  • Genetic homogeneity
  • Iranian family
  • LOD score
  • Linkage analysis
  • Mapping
  • Syndactyly type 1

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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