| Literature DB >> 14661305 |
C Türkay Yalin1, Ilkay Koray Bayrak, Murat Danaci, Lütfi Incesu.
Abstract
Chondrodysplasia punctata is a peroxisomal disorder which is a form of multiple epiphyseal dysplasia. It is characterized by calcifications of unossified cartilaginous epiphyseal centers during the first year of life. Severe autosomal recessive rhisomelic form shows bilateral proximal shortening of the upper and lower limbs with punctate epiphyseal calcifications. We report radiological findings of a patient with rhisomelic chondrodysplasia punctata. Magnetic resonance imaging showed foramen magnum stenosis that caused spinal cord compression.Entities:
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Year: 2003 PMID: 14661305
Source DB: PubMed Journal: Tani Girisim Radyol ISSN: 1300-4360