Richner Hanhart syndrome.

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dc.contributor.authorJanakiraman, Lalithaen_US
dc.contributor.authorSathiyasekaran, Malathien_US
dc.contributor.authorDeenadayalan, Munirathiramen_US
dc.contributor.authorGanesh, Ramaswamyen_US
dc.contributor.authorMahesh, Umaen_US
dc.date.accessioned2006-02-04en_US
dc.date.accessioned2009-05-30T13:16:55Z
dc.date.available2006-02-04en_US
dc.date.available2009-05-30T13:16:55Z
dc.date.issued2006-02-04en_US
dc.description.abstractRichner 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.en_US
dc.description.affiliationKanchi Kamakoti CHILDS Trust Hospital, Chennai, India. jlalitha54@hotmail.comen_US
dc.identifier.citationJanakiraman L, Sathiyasekaran M, Deenadayalan M, Ganesh R, Mahesh U. Richner Hanhart syndrome. Indian Journal of Pediatrics. 2006 Feb; 73(2): 161-2en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/81531
dc.language.isoengen_US
dc.source.urihttps://medind.nic.in/icb/icbai.shtmlen_US
dc.subject.meshEye Diseases --etiologyen_US
dc.subject.meshFemaleen_US
dc.subject.meshHumansen_US
dc.subject.meshInfanten_US
dc.subject.meshSkin Diseases --etiologyen_US
dc.subject.meshTyrosinemias --complicationsen_US
dc.titleRichner Hanhart syndrome.en_US
dc.typeCase Reportsen_US
dc.typeJournal Articleen_US
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