Janakiraman, LalithaSathiyasekaran, MalathiDeenadayalan, MunirathiramGanesh, RamaswamyMahesh, Uma2006-02-042009-05-302006-02-042009-05-302006-02-04Janakiraman L, Sathiyasekaran M, Deenadayalan M, Ganesh R, Mahesh U. Richner Hanhart syndrome. Indian Journal of Pediatrics. 2006 Feb; 73(2): 161-2http://imsear.searo.who.int/handle/123456789/81531Richner 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.engEye Diseases --etiologyFemaleHumansInfantSkin Diseases --etiologyTyrosinemias --complicationsCase Reports