Craniofacial manifestations in osteogenesis imperfecta type III in South Africa

OBJECTIVES: Osteogenesis imperfecta type III (OMIM 259420) is a severe autosomal recessive disorder. Affected individuals have multiple fractures, develop limb deformities with spinal malalignment and stunted stature. MATERIALS AND METHODS: The frequency of Osteogenesis imperfecta type III (OI III)...

Popoln opis

Shranjeno v:
Bibliografske podrobnosti
izdano v:BDJ Open
Main Authors: Chetty, Manogari, Roberts, Tina Sharon, Stephen, Lawrence, Beighton, Peter
Format: Artigo
Jezik:Inglês
Izdano: Nature Publishing Group 2017
Teme:
Article
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC5831017/
https://ncbi.nlm.nih.gov/pubmed/29607091
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/bdjopen.2017.21
Oznake: Označite
Brez oznak, prvi označite!

Podobne knjige/članki