Brittle Bone Disease: A Case Report

pubmed: wnt1 2023-03-21


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...


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

Date tagged:

03/21/2023, 03:16

Date published:

12/12/2022, 06:00