Hartnup disease

An autosomal recessive inherited metabolic disorder caused by mutations in the SLC6A19 gene. It is characterized by defective absorption of neutral amino acids. Signs and symptoms include skin eruptions reminiscent of pellagra, aminoaciduria, and cerebellar ataxia.

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Dharmapuri, Tamil Nadu, India
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Kasturba Medical College, Manipal

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PGIMER, Chandigarh

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Maharaja Gandhi Institute Of Medical Sciences, Sewagram

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Howrah
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Chandigarh, India
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Dehradun
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Pune
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