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

Internet

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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