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 |
Disease | Chanarin-Dorfman syndrome |
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