Definición:
A heterogeneous group of bone dysplasias, the common character of which is stippling of the epiphyses in infancy. The group includes a severe autosomal recessive form (), an autosomal dominant form (Conradi-Hunermann syndrome), and a milder X-linked form. Metabolic defects associated with impaired peroxisomes are present only in the rhizomelic form.
Sinónimos:
Condrodistrofia Calcificante Congénita /
Displasia Epifisaria Punctata /
EpÃfisis Punteada /
Condrodistrofia Calcificante Congenita /
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Termino(s) especÃfico(s): |