A Case of Hereditary Multiple Osteochondromatosis / 대한정형외과학회잡지
The Journal of the Korean Orthopaedic Association
;
: 539-543, 1982.
Artigo
em Coreano
| WPRIM
| ID: wpr-767865
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.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Esqueleto
/
Tíbia
/
Exostose Múltipla Hereditária
/
Fêmur
/
Articulação do Joelho
Limite:
Humanos
Idioma:
Coreano
Revista:
The Journal of the Korean Orthopaedic Association
Ano de publicação:
1982
Tipo de documento:
Artigo
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