Literature DB >> 2363425

Fibular hypoplasia and complex brachydactyly (Du Pan syndrome) in an inbred Pakistani kindred.

M Ahmad1, H Abbas, A Wahab, S Haque.   

Abstract

A Pakistani kindred comprising 7 generations contained 7 men and 2 women with fibular hypoplasia and complex brachydactyly (syn: Du Pan syndrome). Analysis of the pedigree is strongly suggestive of autosomal recessive inheritance. The average inbreeding coefficient (F) for the affected persons was found to be significantly greater than that for unaffected persons in the pedigree and consanguineous loops could account for all affected persons being homozygous for the abnormal allele.

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Year:  1990        PMID: 2363425     DOI: 10.1002/ajmg.1320360309

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  1 in total

1.  A mutation in the receptor binding site of GDF5 causes Mohr-Wriedt brachydactyly type A2.

Authors:  K W Kjaer; H Eiberg; L Hansen; C B van der Hagen; K Rosendahl; N Tommerup; S Mundlos
Journal:  J Med Genet       Date:  2005-07-13       Impact factor: 6.318

  1 in total

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