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CASE REPORT
Year : 2012  |  Volume : 16  |  Issue : 4  |  Page : 643-645

Homozygous familial hypercholesterolemia


Department of Pediatrics, S.M.G.S Hospital, G.M.C Jammu, Jammu and Kashmir, India

Correspondence Address:
Ravi Kumar Parihar
Department of Pediatrics, S.M.G.S Hospital, Government Medical College Jammu, Jammu and Kashmir - 180 001
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/2230-8210.98032

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Familial hypercholesterolema (FH) is an inherited autosomal dominant disorder of lipid metabolism. We report a 3 years old female child who presented with multiple eruptive xanthomatosis of skin since 6 months of age and had deranged lipid profile consistent with FH.


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