Brittle Bone Brothers: Osteogenesis Imperfecta Conventional Serial Case

Osteogenesis Imperfecta is a hereditary connective tissue disorder due to COL1A1/2 mutation causing gene defect encoding proteins to metabolize collagen. The skeletal manifestation of OI causing bone incompetence, hence the name brittle bone disease. Here we report three cases of OI type IV in adult...

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Bibliographic Details
Main Authors: Marsha Ruthy Darmawan, Elysanti Dwi Maharani
Format: Article
Language:English
Published: State Islamic University Sunan Kalijaga 2021-07-01
Series:Biology, Medicine & Natural Product Chemistry
Subjects:
Online Access:http://sciencebiology.org/index.php/BIOMEDICH/article/view/125