Literature DB >> 1308362

De Barsy syndrome: report of a case, literature review, and elastin gene expression studies of the skin.

P S Karnes1, A T Shamban, D R Olsen, M J Fazio, R E Falk.   

Abstract

Several "progeroid" syndromes have now been identified. The De Barsy syndrome is an autosomal recessive syndrome of dwarfism, mental deficiency, an "aged" appearance at birth, abnormal elastic fibers on skin biopsy, and lax skin, large helices, eye abnormalities, lax joints, hypotonia, and athetoid posturing. We report one case and review 11 cases from the literature. To understand the abnormal appearance of the elastic fibers on biopsy, we performed elastin gene expression studies on fibroblasts cultured from our patient's skin. Molecular hybridization studies revealed reduced elastin mRNA steady-state levels as compared with age matched control individuals. Assuming normal rates of mRNA translation, reduced elastin synthesis would occur. Diminished dermal elastin content could explain the altered cutaneous elasticity, decreased elastic fibers in the skin, and many clinical manifestations of individuals with this condition.

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Year:  1992        PMID: 1308362     DOI: 10.1002/ajmg.1320420108

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


  1 in total

1.  A 5-year Journey with Cutis Laxa in an Indian Child: The De Barsy Syndrome Revisited.

Authors:  Abhijit Dutta; Sudip Kumar Ghosh; Arghyaprasun Ghosh; Sutirtha Roy
Journal:  Indian J Dermatol       Date:  2016 Jan-Feb       Impact factor: 1.494

  1 in total

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