Plain radiographic diagnosis of 'osteogenesis imperfecta congenita' (Type III) in a 2-year-old boy

Autor:	Bello O Usman, Fatai A Oyewole, Lawal Suleiman
Rok vydání:	2021
Předmět:	Pediatrics medicine.medical_specialty Growth retardation Black african Bone disease business.industry Osteogenesis imperfecta Radiography medicine Bone fragility OSTEOGENESIS IMPERFECTA CONGENITA business medicine.disease
Zdroj:	Journal of Radiation Medicine in the Tropics. 2:40
ISSN:	2667-2537
DOI:	10.4103/jrmt.jrmt_28_20
Popis:	Osteogenesis imperfecta (OI), or brittle bone disease, is a rare disorder with congenital bone fragility caused by mutations in the genes. This case is reported because of its rarity and paucity in the literature in Nigeria. Available data on OI in Black African children are limited.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::c1d90fca4b29351b44ba9fb0ee27853f https://doi.org/10.4103/jrmt.jrmt_28_20 Zobrazit plný text záznamu