Neutral lipid storage disease. Case report and lipid studies.

Judge, M R; Atherton, D J; Salvayre, R; Hilaire, N; Levade, T; Johnston, D I; Winchester, B; Lake, B D · Br J Dermatol · 1994

case_report · Level V

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Abstract

A 9-year-old boy of Greek-Cypriot origin had been diagnosed at the age of 3 years as suffering from non-bullous ichthyosiform erythroderma. However, he also had hepatomegaly and abnormal liver function tests, biochemical evidence of myopathy, early cataracts, and lipid vacuoles in white blood cells and basal keratinocytes. A diagnosis of neutral lipid (triglyceride) storage disease was confirmed by lipid studies on cultured fibroblasts.

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