Literature DB >> 104811

Variable expression in a dominantly inherited skeletal dysplasia with similarities to brachydactyly E and spondyloepiphyseal-spondyloperipheral dysplasia.

V P Sybert, P H Byers, J G Hall.   

Abstract

Variable expression and penetrance of dominantly inherited disorders present problems in diagnosis and counseling. The variation in clinical findings within a family with an autosomal dominant skeletal dysplasia is presented. In some members only shortened metacarpals were found, as seen in classic Brachydactyly E. Others presented with more severe and generalized skeletal involvement, such as is found in some of the spondyloepiphyseal dysplasias. This family may represent the true spectrum of Brachydactyly E; they may be affected with a specific spondyloepiphyseal dysplasia; or they may represent a new syndrome. The authors favor the first possibility and feel that this family serves to emphasize the importance of examining all affected members in a kindred with an autosomal dominant disease.

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Year:  1979        PMID: 104811     DOI: 10.1111/j.1399-0004.1979.tb01755.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  2 in total

1.  Spondyloepiphyseal dysplasia.

Authors:  J Vanĕk
Journal:  J Med Genet       Date:  1983-04       Impact factor: 6.318

2.  Spondyloepiphyseal dysplasia and precocious osteoarthritis in a family with an Arg75-->Cys mutation in the procollagen type II gene (COL2A1).

Authors:  C J Williams; E L Considine; R G Knowlton; A Reginato; G Neumann; D Harrison; P Buxton; S Jimenez; D J Prockop
Journal:  Hum Genet       Date:  1993-11       Impact factor: 4.132

  2 in total

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