Category:Sjögren–Larsson syndrome

**Sjogren-Larsson syndrome**
	autosomal recessive form of ichthyosis apparent at birth
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Instance of	rare disease; class of disease;
Subclass of	autosomal recessive disease; neurometabolic disease; disorder of phospholipids, sphingolipids and fatty acids biosynthesis with central nervous system predominant involvement; autosomal ichthyosis syndrome with prominent neurological signs; unclassified primitive or secondary maculopathy; metabolic disease with cataract; metabolic disease with pigmentary retinitis; syndromic ichthyosis associated with ocular features; hereditary retinal dystrophy; syndromic dyslipidemia; syndrome; disease;
Named after	Torsten Sjögren;
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	Q2291208;
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