A Case of Hereditary Multiple Osteochondromatosis / 대한정형외과학회잡지
The Journal of the Korean Orthopaedic Association
; : 539-543, 1982.
Article
in Korean
| WPRIM (Western Pacific)
| ID: wpr-767865
Responsible library:
WPRO
ABSTRACT
Multiple osteochondromatosis is a hereditary disorder affecting the endochondral skeleton during period of growth. We have studied a family which have multiple osteochondromatosis clinically and radiologically. In this family, eight of ten members could traceable, have the lesions of multiple osteochondromatosis. The most common site of the lesions was in femur, and the next common site was in tibia, especially, near the knee joint.
Full text:
Available
Database:
WPRIM (Western Pacific)
Main subject:
Skeleton
/
Tibia
/
Exostoses, Multiple Hereditary
/
Femur
/
Knee Joint
Limits:
Humans
Language:
Korean
Journal:
The Journal of the Korean Orthopaedic Association
Year:
1982
Document type:
Article