Venencie_1988_Pediatr.Dermatol_5_173

Reference

Title : Ichthyosis and neutral lipid storage disease (Dorfman-Chanarin syndrome) - Venencie_1988_Pediatr.Dermatol_5_173
Author(s) : Venencie PY , Armengaud D , Foldes C , Vieillefond A , Coulombel L , Hadchouel M
Ref : Pediatr Dermatol , 5 :173 , 1988
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.

PubMedSearch : Venencie_1988_Pediatr.Dermatol_5_173
PubMedID: 3205858

Related information

Citations formats

Venencie PY, Armengaud D, Foldes C, Vieillefond A, Coulombel L, Hadchouel M (1988)
Ichthyosis and neutral lipid storage disease (Dorfman-Chanarin syndrome)
Pediatr Dermatol 5 :173

Venencie PY, Armengaud D, Foldes C, Vieillefond A, Coulombel L, Hadchouel M (1988)
Pediatr Dermatol 5 :173