Richner Hanhart syndrome.
作者信息
Janakiraman Lalitha, Sathiyasekaran Malathi, Deenadayalan Munirathiram, Ganesh Ramaswamy, Mahesh Uma
机构信息
Kanchi Kamakoti CHILDS Trust Hospital, Chennai, India.
出版信息
Indian J Pediatr. 2006 Feb;73(2):161-2. doi: 10.1007/BF02820213.
PMID:16514229
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.
摘要
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