Literature DB >> 3205858

Ichthyosis and neutral lipid storage disease (Dorfman-Chanarin syndrome).

P Y Venencie1, D Armengaud, C Foldès, A Vieillefond, L Coulombel, M Hadchouel.   

Abstract

Ichthyosis and neutral lipid storage disease (INLSD) is a nonlysosomal, multisystemic, triglyceride storage disorder. It is characterized by nonbullous congenital ichthyosiform erythroderma (NBCIE), leukocyte vacuoles, and variable involvement of the liver, muscles, eyes, and central nervous system. In our patient fat-containing vacuoles were also demonstrated in the epidermis. In patients with NBCIE, the diagnosis of INLSD is readily made by direct examination of a peripheral blood smear demonstrating cytoplasmic lipid vacuoles within most granulocytes and monocytes.

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Year:  1988        PMID: 3205858     DOI: 10.1111/j.1525-1470.1988.tb01165.x

Source DB:  PubMed          Journal:  Pediatr Dermatol        ISSN: 0736-8046            Impact factor:   1.588


  2 in total

1.  Mutations in CGI-58, the gene encoding a new protein of the esterase/lipase/thioesterase subfamily, in Chanarin-Dorfman syndrome.

Authors:  C Lefèvre; F Jobard; F Caux; B Bouadjar; A Karaduman; R Heilig; H Lakhdar; A Wollenberg; J L Verret; J Weissenbach; M Ozgüc; M Lathrop; J F Prud'homme; J Fischer
Journal:  Am J Hum Genet       Date:  2001-10-02       Impact factor: 11.025

2.  A rare cause of Fatty liver and elevated aminotransferase levels: chanarin-dorfman syndrome: a case report.

Authors:  Ozdal Ersoy; Canan Alkım; Mehmet Derya Onuk; Hüseyin Demirsoy; Dilek Argon
Journal:  Int J Hepatol       Date:  2011-01-20
  2 in total

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