Condrodisplasia metafisária tipo Schmid - Tratamento de deformidade do joelho por hemiepifisiodese tipo Métaizeau
DOI:
https://doi.org/10.61443/rto.v23i2.425Keywords:
condrodisplasia metafisária tipo Schmid; coxa vara; hemiepifisiodese temporária.Abstract
Schmid-type metaphyseal chondrodysplasia is a genetic disease of autosomal
dominant pattern, caused by a mutation in the gene encoding type X collagen. It
has been described an incidence of 3-6 cases per million people and is
characterized by the appearance around 2 years of progressive short stature,
swinging gait and marked lumbar lordosis. The case described is of an 8-yearold patient referred to the Pediatric Orthopedics outpatient clinic of Hospital Santa
Lucinda, Sorocaba - SP, with a classic picture of this disease, with lower limbs
arching, short stature (between percentile 3 and 10), marked lumbar lordosis by
thigh stick and swinging gait. She undenwent temporary hemiepiphysiodesis of
the tibia, with varus deformity correction.
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References
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