A Four and a alf Year Old Boy with Myositis Ossificans Progressiva

dc.contributor.author	Amarasena, S.
dc.contributor.author	Samanlatha, M.G.K.
dc.contributor.author	De Silva, M.H.A.D.
dc.contributor.author	Kolombage, P.
dc.date.accessioned	2023-05-30T03:48:35Z
dc.date.available	2023-05-30T03:48:35Z
dc.date.issued	2009-09
dc.identifier.uri	http://ir.lib.ruh.ac.lk/xmlui/handle/iruor/12875
dc.description.abstract	Myositis ossificans progressiva (MOP) (synonymous with fibrodysplasia ossificans progressiva) is an extremely rare disease inherited in an autosomal dominant manner with an estimated incidence of 0.1 per one million births1. The diagnosis can be difficult due to its rare nature and different manifestations early in the illness. No detailed descriptions are available in standard reference texts2.	en_US
dc.language.iso	en	en_US
dc.publisher	Faculty of Medicine, University of Ruhuna, Galle, Sri Lanka	en_US
dc.subject	Myositis ossificans progressiva	en_US
dc.subject	MOP	en_US
dc.subject	fibrodysplasia ossificans progressiva	en_US
dc.title	A Four and a alf Year Old Boy with Myositis Ossificans Progressiva	en_US
dc.type	Article	en_US