Title of article
Neutral lipid storage disease-a case report
Author/Authors
Butt, Ghazala King Edward Medical University - Mayo Hospital - Department of Dermatology, Unit II, Pakistan , Bano, Asia King Edward Medical University - Mayo Hospital - Department of Dermatology, Unit II, Pakistan , Pal, Sabrina Suhail King Edward Medical University - Mayo Hospital - Department of Dermatology, Unit II, Pakistan , Khurshid, Khawar King Edward Medical University - Mayo Hospital - Department of Dermatology, Unit II, Pakistan , Asad, Faria King Edward Medical University - Mayo Hospital - Department of Dermatology, Unit II, Pakistan , Rani, Zahida King Edward Medical University - Mayo Hospital - Department of Dermatology, Unit II, Pakistan
From page
176
To page
179
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.
Keywords
Neutral lipid storage disease , non , bullous ichthyosiform erythroderma , Jordan’s anomaly.
Journal title
Journal of Pakistan Association of Dermatologists
Journal title
Journal of Pakistan Association of Dermatologists
Record number
2584331
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