Literature DB >> 6237581

Presumed homozygous Ehlers-Danlos syndrome type I in a highly inbred kindred.

S I Kozlova, A N Prytkov, O E Blinnikova, F A Sultanova, D N Bochkova.   

Abstract

While studying an extended family of individuals with the Ehlers-Danlos (ED) syndrome type I, we found an affected male who was born to 2 affected consanguineous parents. This man had a more severe condition than that of his other affected relatives. Moreover, all 6 of his children were affected. Taking the pedigree data into account, the conditional probability of homozygosity for the ED gene in that patient was calculated as 97%. Some problems of the clinical and genetic approach to the recognition of the homozygous state in the ED syndrome are discussed using this family as an example.

Entities:  

Mesh:

Year:  1984        PMID: 6237581     DOI: 10.1002/ajmg.1320180423

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


  1 in total

1.  Exclusion of COL1A1, COL1A2, and COL3A1 genes as candidate genes for Ehlers-Danlos syndrome type I in one large family.

Authors:  B P Sokolov; A N Prytkov; G Tromp; R G Knowlton; D J Prockop
Journal:  Hum Genet       Date:  1991-12       Impact factor: 4.132

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.