Journal of South Asian Federation of Obstetrics and Gynaecology

Register      Login

VOLUME 2 , ISSUE 1 ( January-April, 2010 ) > List of Articles

CASE REPORT

Osteogenesis Imperfecta with Chondrodysplasia Punctata: A New Syndrome

Sabahat Rasool, Amir Qamar, Omar Salim Akhtar

Citation Information : Rasool S, Qamar A, Akhtar OS. Osteogenesis Imperfecta with Chondrodysplasia Punctata: A New Syndrome. J South Asian Feder Obs Gynae 2010; 2 (1):59-61.

DOI: 10.5005/jp-journals-10006-1062

Published Online: 01-08-2012

Copyright Statement:  Copyright © 2010; The Author(s).


Abstract

PDF Share
  1. Prenatal diagnosis of osteogenesis imperfecta type II. Int J Gynecol Obstet 1998;61:33-38.
  2. International classification of osteochondrodysplasias. International Working Group on Constitutional Diseases of Bone. Am J Med Genet 1992;44:223-29.
  3. Osteogenesis imperfecta nasology and genetics. In: Cetta G, Ramirez F, Tsipouras P (Eds). Third International Conference on Osteogenesis Imperfecta. New York, NY: New York Academy of Sciences 1998;543:4-8.
  4. Trisomy of chromosomes 13-15 and 17-18: Its association with infantile arteriosclerosis. Am J Med Sci 1962;244:763-79.
  5. Skin manifestations of Conradi's disease: Chondrodystrophia congenital punctata. Arch Derm 1996;94:743-48.
  6. Genetic and biochemical heterogeneity in patients with the rhizomelic form of chondrodysplasia punctata: A complementation study. Hum Genet 1992;89:439-44.
  7. A new type of chondrodysplasia punctata associated with peroxisomal dysfunction. J Inherit Metab Dis 1991;14:361-63.
PDF Share
PDF Share

© Jaypee Brothers Medical Publishers (P) LTD.