Osteogenesis imperfecta: a case report
Article
| IMSEAR
| ID: sea-204271
ABSTRACT
Osteogenesis imperfecta (OI) is a group of rare inherited disorders of connective tissue with the common feature of excessive fragility of bones caused by mutations in collagen. Diagnosis is mainly based on the clinical features of the disorder. We report a late preterm a male neonate born to a 20 years old primigravida. He had clinical features of a type II OI and severe birth asphyxia.
Full text:
Available
Index:
IMSEAR (South-East Asia)
Year:
2019
Type:
Article
Similar
MEDLINE
...
LILACS
LIS