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Brittle bone disease
Description:
Brittle bone disease. Image 2 of 2. Patient with severe osteogenesis imperfecta (OI). OI is a brittle bone disorder, caused by a dominant genetic mutation of the gene for collagen, a vital protein found in bones. Sufferers either have too little, or have poor quality collagen. Consequently the skeleton is fragile and prone to multiple broken and fractured bones. In severe cases of OI, as here, the patient has a barrel-chest, spinal curvature, severe bone deformities, loose joints, and poor muscle development in the limbs. There is no treatment for OI. See M230/345 for a view of the same patient from the front.
Credit:
Dr M.A. Ansary/Science Source
Unique identifier:
SS2177806
Legacy Identifier:
SC9926
Type:
Image
Size:
2443px × 3750px (~26 MB)
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Tags
adolescent
africa
black
bones
boy
brittle bone disease
collagen
condition
deficiency
deformed
deformity
develop
disability
disabled
disease
disorder
E03301
genetic
human
human body
inherited
M230/0346
M230/346
M2300346
male
medicine
mutation
oi
one
osteogenesis imperfecta
osteology
patient
person
portrait
severe
single
third world
vertical