A case of Revesz syndrome

dc.contributor.author	Kankananarachchi, C. I.
dc.contributor.author	Wickramasinghe, N. D.
dc.contributor.author	Vithana, S. R.
dc.contributor.author	Munasinghe, T. M.
dc.contributor.author	Amarasena, S.
dc.date.accessioned	2023-05-29T04:17:59Z
dc.date.available	2023-05-29T04:17:59Z
dc.date.issued	2018-06-05
dc.identifier.uri	http://ir.lib.ruh.ac.lk/xmlui/handle/iruor/12868
dc.description.abstract	Classical features of Revesz syndrome (RS) include skin pigmentation, nail dystrophy, oral leukoplakia, cerebellar hypoplasia, growth retardation and delayed psychomotor development1. We report a child with RS with classical multisystem involvement.	en_US
dc.language.iso	en	en_US
dc.publisher	Faculty of Medicine, University of Ruhuna, Galle, Sri Lanka	en_US
dc.subject	Revesz syndrome	en_US
dc.subject	Dyskeratosis congenita	en_US
dc.subject	Pancytopenia	en_US
dc.subject	Cerebellar hypoplasia	en_US
dc.subject	Nail dystrophy	en_US
dc.title	A case of Revesz syndrome	en_US
dc.type	Article	en_US