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Neutral lipid storage disease-a case report.

Author(s)
Ghazala Butt Department of Dermatology, Unit II, King Edward Medical University/Mayo Hospital, Lahore, Pakistan
Asia Bano Department of Dermatology, Unit II, King Edward Medical University/Mayo Hospital, Lahore, Pakistan
Sabrina Suhail Pal Department of Dermatology, Unit II, King Edward Medical University/Mayo Hospital, Lahore, Pakistan
Khawar Khurshid Department of Dermatology, Unit II, King Edward Medical University/Mayo Hospital, Lahore, Pakistan
Faria Asad Department of Dermatology, Unit II, King Edward Medical University/Mayo Hospital, Lahore, Pakistan
Zahida Rani Department of Dermatology, Unit II, King Edward Medical University/Mayo Hospital, Lahore, Pakistan
Abstract
Neutral lipid storage disease is a rare autosomal recessive disorder characterized by non-bullous ichthyosiform erythroderma, liver steatosis, hepatosplenomegaly, cataracts, ataxia, bilateral sensorineural hearing loss, skeletal and cardiomyopathy, growth and mental retardation. We report a case of neutral lipid storage disease in a 14 months old child.
Publication Details
Page(s) 176-179
DOI DOI not available
Published Journal: Journal of Pakistan Association of Dermatologists, Volume: 24, Issue: 2, Year: 2014

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