Literature DB >> 3354610

Ichthyosis and neutral lipid storage disease.

S Musumeci1, A D'Agata, C Romano, R Patané, D Cutrona.   

Abstract

A boy with a lipid storage disease characterized by lamellar ichthyosis, cataracts, hepatosplenomegaly, and leukocyte vacuoles has been identified in a Sicilian family. This patient shows all the characteristics of ichthyosis and neutral lipid storage disease (Chanarin-Dorfman syndrome). Family data confirm an autosomal recessive inheritance; the heterozygotes may be detected by the presence of vacuoles in circulating eosinophils.

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Year:  1988        PMID: 3354610     DOI: 10.1002/ajmg.1320290219

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


  3 in total

1.  Comments on Jordans' anomaly.

Authors:  M S Tullu; M N Muranjan; C T Deshmukh
Journal:  Indian J Pediatr       Date:  2000-09       Impact factor: 1.967

2.  Comparative gene identification-58 (CGI-58) promotes autophagy as a putative lysophosphatidylglycerol acyltransferase.

Authors:  Jun Zhang; Dan Xu; Jia Nie; Ruili Han; Yonggong Zhai; Yuguang Shi
Journal:  J Biol Chem       Date:  2014-10-14       Impact factor: 5.157

3.  CGI-58, the causative gene for Chanarin-Dorfman syndrome, mediates acylation of lysophosphatidic acid.

Authors:  Ananda K Ghosh; Geetha Ramakrishnan; Chitraju Chandramohan; Ram Rajasekharan
Journal:  J Biol Chem       Date:  2008-07-07       Impact factor: 5.157

  3 in total

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