| Literature DB >> 3354610 |
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.Entities:
Mesh:
Year: 1988 PMID: 3354610 DOI: 10.1002/ajmg.1320290219
Source DB: PubMed Journal: Am J Med Genet ISSN: 0148-7299