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
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.
