Brittle Bone Disease: A Case Report

pubmed: wnt1 2023-03-17

Summary:

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 and had an uneventful pregnancy. In delivery, the newborn suffered bilateral collarbone fractures. After a week, she returned to an unscheduled appointment at the healthcare family unit due to an...

Link:

https://pubmed.ncbi.nlm.nih.gov/36505123/?utm_source=Other&utm_medium=rss&utm_campaign=None&utm_content=16uwQpOeqFYN8R4TKOtwPy2utpqy9ex2oldalD2yF_fQHv2caq&fc=None&ff=20230317111601&v=2.17.9.post6+86293ac

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Authors:

Tatiana Luis, Ana Cristina Gonçalves, Eduardo Rodrigues, Maricela Mendes, Tânia Teixeira

Date tagged:

03/17/2023, 11:16

Date published:

12/12/2022, 06:00