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Brittle Bone Disease: A Case Report

Osteogenesis imperfecta (OI) is a rare genetic disorder. Due to considerable phenotypic variability, a classification was developed for OI subtypes based on clinical features and disease severity. A seven-day-old female was born at 40+1 weeks of gestation whose mother received routine antenatal care...

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Detalles Bibliográficos
Autores principales:	Luis, Tatiana, Gonçalves, Ana Cristina, Rodrigues, Eduardo, Mendes, Maricela, Teixeira, Tânia
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Cureus 2022
Materias:	Family/General Practice
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9731666/ https://www.ncbi.nlm.nih.gov/pubmed/36505123 http://dx.doi.org/10.7759/cureus.31259

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