Chanarin-Dorfman syndrome: Clinical features of a rare lipid metabolism disorder

Pediatric Dermatology

Volumn 26, Issue 1, 2009, Pages 40-43

  Selimoglu, Mukadder Ayse ^a   Esrefoglu, Mukaddes ^a   Gul, Mehmet ^a   Gungor, Serdal ^a   Yildirim, Cigdem ^a   Seyhan, Muammer ^a  

^a INONU UNIVERSITY   (Turkey)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA TOCOPHEROL; EMOLLIENT AGENT; URSODEOXYCHOLIC ACID;

ARTICLE; AUTOSOMAL DISORDER; BLOOD SMEAR; CASE REPORT; CELL VACUOLE; CHANARIN DORFMAN SYNDROME; CHILD; CLINICAL ASSESSMENT; CLINICAL FEATURE; CONGENITAL ICHTHYOSIFORM ERYTHRODERMA; DISORDERS OF LIPID AND LIPOPROTEIN METABOLISM; ELECTRON MICROSCOPE; FATTY LIVER; FEMALE; HUMAN; HUMAN TISSUE; LIVER BIOPSY; LIVER DISEASE; NEUTROPHIL; PRIORITY JOURNAL; SCHOOL CHILD; SCREENING; SKIN BIOPSY; SKIN DISEASE; ULTRASTRUCTURE;

CHILD; FEMALE; HUMANS; ICHTHYOSIFORM ERYTHRODERMA, CONGENITAL; KERATINOCYTES; LIPID METABOLISM, INBORN ERRORS; MICROSCOPY, ELECTRON; NEUTROPHILS; SKIN;

EID: 60449093396     PISSN: 07368046     EISSN: 15251470     Source Type: Journal    
DOI: 10.1111/j.1525-1470.2008.00818.x     Document Type: Article

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