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A Case of Hereditary Multiple Osteochondromatosis / 대한정형외과학회잡지
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.
Subject(s)

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
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
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