J Korean Pediatr Soc.  1994 Sep;37(9):1312-1316.

A Case of Rhizomelic Chondrodysplasia Punctata

Abstract

Chondrodysplasia punctata is a rare congenital disorder of bone, occuring in infants, which is characterized by radiographic manifestation of premature deposition of punctate calcific densitiy in epiphyseal areas, preformed in cartilage. We experienced a case of rhizomelic type-chondrodysplsia punctata in a two day old female who showed short stature, symmetric shortening of proximal limbs, cataract, icthyositic skin lesion and characteristic coronal clefts in lumbar vertebral bodies on X-ray.


MeSH Terms

Cartilage
Cataract
Chondrodysplasia Punctata
Chondrodysplasia Punctata, Rhizomelic*
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Extremities
Female
Humans
Infant
Skin
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