Chanarin-Dorfman Syndrome: Clinical Features of a Rare Lipid Metabolism

dc.contributor.author	Selimoglu, MA
dc.contributor.author	Esrefoglu, M
dc.contributor.author	Gul, M
dc.contributor.author	Gungor, S
dc.contributor.author	Yildirim, C
dc.contributor.author	Seyhan, M
dc.date.accessioned	2022-03-28T11:38:08Z
dc.date.available	2022-03-28T11:38:08Z
dc.date.issued	2009
dc.identifier.uri	http://hdl.handle.net/11616/57901
dc.description.abstract	Chanarin-Dorfman syndrome (CDS) is a very rare neutral lipid metabolism disorder with multisystem involvement. In order to not underdiagnose the cases, screening of lipid vacuoles in neutrophils from peripheral blood smears in patients with ichthyosiform erythroderma is needed. Few case reports revealing ultrastructural findings of skin and especially liver in that disorder were observed. Here we discuss clinical and electron microscopic findings of two siblings with CDS.
dc.source	PEDIATRIC DERMATOLOGY
dc.title	Chanarin-Dorfman Syndrome: Clinical Features of a Rare Lipid Metabolism
dc.title	Disorder

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