Schmid Type of Metaphyseal Chondrodysplasia: 17 years Follow-up Case / 대한정형외과학회잡지
The Journal of the Korean Orthopaedic Association
;
: 567-570, 2002.
Article
in Korean
| 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.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Osteotomy
/
Congenital Abnormalities
/
Follow-Up Studies
/
Dwarfism
/
Genetic Diseases, Inborn
Type of study:
Observational study
/
Prognostic study
Limits:
Humans
/
Male
Language:
Korean
Journal:
The Journal of the Korean Orthopaedic Association
Year:
2002
Type:
Article
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