Schmid Type of Metaphyseal Chondrodysplasia with COL10A1 Mutation
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Poster Presentations
P: 13-13
June 2017

Schmid Type of Metaphyseal Chondrodysplasia with COL10A1 Mutation

1. Van Training And Research Hospital, Clinic Of Pediatric Endocrinology, Van, Turkey
2. Selçuk University Faculty Of Medicine, Department Of Pediatric Endocrinology, Konya, Turkey
3. Firat University Faculty Of Medicine, Department Of Medical Genetics, Elazig, Turkey
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The Schmid type of metaphyseal chondrodysplasia (MCDS) is characterized by short stature, widened growth plates, and bowing of the long bones, resulting from autosomal dominant mutations of COL10A1.

We report a patient with MCDS and COL10A1 mutation.

A 4-year 7-month-old boy was referred to our hospital because of bowing of the legs and short stature. His mother showed short stature and bowing of the legs, too. His height and weight were 75 cm (<3th p) (-2 SDS) and 21.6 kg (75-90th p), respectively. Ca, P, ALP, PTH, and 25-OH D levels were normal. Radiographs showed findings compatible with MCDS. p.W651*(c.1952G>A)(heterozygote) mutation in the COL10A1 gene was identified. The patient was diagnosed with MCDS.

We report this patient with MCDS and COL10A1 mutation as it is a rarely seen case.