Childhood Osteoporosis and Presentation of Two Cases with Osteogenesis Imperfecta Type V

INTRODUCTION: Osteogenesis imperfecta (OI) is etiologically heterogeneous disorder characterized by childhood osteoporosis. A subtype OI type V is caused by the same c.-14C>T mutation in the IFITM5 gene. Nevertheless, there is a marked interindividual phenotypic variability in clinical presentati...

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Publicado en:Zdr Varst
Main Authors: BRATANIC, Nina, DZODAN, Bojana, TREBUSAK PODKRAJSEK, Katarina, BERTOK, Sara, OSTANEK, Barbara, MARC, Janja, BATTELINO, Tadej, AVBELJ STEFANIJA, Magdalena
Formato: Artigo
Idioma:Inglês
Publicado: De Gruyter Open 2015
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Original Scientific Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC4820164/
https://ncbi.nlm.nih.gov/pubmed/27646918
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1515/sjph-2015-0018
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