Richner Hanhart syndrome.

Janakiraman, Lalitha; Sathiyasekaran, Malathi; Deenadayalan, Munirathiram; Ganesh, Ramaswamy; Mahesh, Uma

Richner Hanhart syndrome.

Date

2006-02-04

Authors

Janakiraman, Lalitha

Sathiyasekaran, Malathi

Deenadayalan, Munirathiram

Ganesh, Ramaswamy

Mahesh, Uma

Abstract

Richner Hanhart syndrome is a rare inherited disorder involving the metabolism of tyrosine, a semi-essential amino acid and it should be considered in the differential diagnosis of a child presenting with ocular and skin lesions. We report a case of Richner Hanhart syndrome in a 19-month-old child, who presented with ocular and skin lesions.

Citation

Janakiraman L, Sathiyasekaran M, Deenadayalan M, Ganesh R, Mahesh U. Richner Hanhart syndrome. Indian Journal of Pediatrics. 2006 Feb; 73(2): 161-2

URI

https://imsear.searo.who.int/handle/123456789/81531

Collections

Indian Journal of Pediatrics

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