dorfman-chanarin syndrome

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ID: 251724
2007
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Ranked #318 of 318 articles by views in crystallization of organic compounds: an industrial perspective

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Abstract
A four-year-old girl was brought to the dermatology outpatient department with scaling all over the body since birth. She had history of episodic vomiting and abdominal distension. A dermatological diagnosis of lamellar ichthyosis was made. Abdominal examination revealed a nontender hepatomegaly, fatty liver on ultrasonography and deranged liver function tests. Peripheral blood smear showed lipid vacuoles in the granulocytes consistent with Jordans′ anomaly. Similar lipid vacuoles were seen in the basal layer in skin biopsy. An inflammatory infiltrate, moderate fibrosis in the portal tract and diffuse severe fatty change in hepatocytes were seen in liver biopsy. The patient was diagnosed as a case of Dorfman-Chanarin syndrome.
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vijay2007indiandorfman-chanarin Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors ;Gandhi Vijay;Aggarwal Puneet;Dhawan Jyoti;Singh Usha;Bhattacharya S
Journal crystallization of organic compounds: an industrial perspective
Year 2007
DOI
DOI not found
URL
http://www.ijdvl.com/article.asp?issn=0378-6323;year=2007;volume=73;issue=1;spage=36;epage=39;aulast=Gandhi
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