| 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 | 2023-06-02T04:02:54Z | |
| dc.date.available | 2023-06-02T04:02:54Z | |
| dc.date.issued | 2009-07 | |
| dc.identifier.uri | http://ir.lib.ruh.ac.lk/xmlui/handle/iruor/12941 | |
| dc.description.abstract | Acrodysostosis is a rare disease, first described in 1968, characterized by short hands and feet with peripheral dysostosis, small nose and mental retardation1. Although inherited as an autosomal dominant disorder2 most are new mutations. There are just over 50 published cases2. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | Faculty of Medicine, University of Ruhuna, Galle, Sri Lanka | en_US |
| dc.subject | Acrodysostosis | en_US |
| dc.subject | short stature | en_US |
| dc.subject | exostoses | en_US |
| dc.title | A 12 Year Old Girl with Acrodysostosis: a rare Cause of Short Stature | en_US |
| dc.type | Article | en_US |