Literature DB >> 8588574

Spondyloperipheral dysplasia.

G Sorge1, M Ruggieri, R S Lachman.   

Abstract

We present a patient with spondyloperipheral dysplasia, a rare skeletal dysplasia which is characterized by vertebral body abnormalities (platyspondyly, end-plate indentations) and brachydactyly. Our patient also manifested a characteristic "pugilistic" face, sensorineural deafness and mental retardation. This chondroosseous dysplasia appears to be inherited as an autosomal dominant disorder. It appears that there is considerable clinical variability in spondyloperipheral dysplasia.

Entities:  

Mesh:

Year:  1995        PMID: 8588574     DOI: 10.1002/ajmg.1320590204

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  1 in total

1.  Prenatal manifestation and management of a mother and child affected by spondyloperipheral dysplasia with a C-propeptide mutation in COL2A1: case report.

Authors:  Maria Francesca Bedeschi; Vera Bianchi; Barbara Gentilin; Lorenzo Colombo; Federica Natacci; Sabrina Giglio; Elena Andreucci; Laura Trespidi; Barbara Acaia; Andrea Superti Furga; Faustina Lalatta
Journal:  Orphanet J Rare Dis       Date:  2011-02-28       Impact factor: 4.123

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.