Schmid Type of Metaphyseal Chondrodysplasia: 17 years Follow-up Case / 대한정형외과학회잡지
The Journal of the Korean Orthopaedic Association
;
: 567-570, 2002.
Artigo
em Coreano
| WPRIM
| ID: wpr-648173
ABSTRACT
Metaphyseal chondrodysplasia (MCD) is a relatively rare hereditary disease of the skeletal system, in which disproportionate dwarfism sparing the trunk is noted. Among the four subtypes of MCD, the Schmid type is relatively common and shows minimal clinical abnormalities. We report a boy, diagnosed to have MCD, Schmid type, and who was followed-up for 17 years until skeletal maturity, during this period he underwent proximal femoral valgus osteotomies as well as tibial deformity correction with lengthening and femoral lengthening procedures.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Osteotomia
/
Anormalidades Congênitas
/
Seguimentos
/
Nanismo
/
Doenças Genéticas Inatas
Tipo de estudo:
Estudo observacional
/
Estudo prognóstico
Limite:
Humanos
/
Masculino
Idioma:
Coreano
Revista:
The Journal of the Korean Orthopaedic Association
Ano de publicação:
2002
Tipo de documento:
Artigo
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