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...
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 |
Similar Items
-
Dentinogenesis imperfecta associated with osteogenesis imperfecta
by: Mina Biria, et al.
Published: (2012-01-01) -
Osteogenesis Imperfecta in Pregnancy: Case Report
by: Maryam Rabiee, et al.
Published: (2011-03-01) -
OSTEOGÉNESIS IMPERFECTA
by: Angélica Ibáñez, et al.
Published: (2021-05-01) -
New 3D Cone Beam CT Imaging Parameters to Assist the Dentist in Treating Patients with Osteogenesis Imperfecta
by: Daniela Messineo, et al.
Published: (2020-12-01) -
Syndromes with congenital brittle bones
by: Plotkin Horacio
Published: (2004-08-01)