Volume 13, Issue 38 (Mar 2003)                   J Mazandaran Univ Med Sci 2003, 13(38): 81-84 | Back to browse issues page

XML Persian Abstract Print

Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Haydaryan F, Silanyan tosi F. Case report on schmid type metaphyseal chondrodysplasia . J Mazandaran Univ Med Sci. 2003; 13 (38) :81-84
URL: http://jmums.mazums.ac.ir/article-1-752-en.html
Abstract:   (9411 Views)
Mataphyseal chondrodysplasia is a term for group of dysplasias, characterized by radiographic changes in metaphyse tubular bones with normal epiphysis. Ït has various types with the name of Schmid type Janson and Mckusis. Schmid type metaphyseal chondrodysplasia is more common in infants, characterized by slight to moderate hieght, bending of limbs and waddling gate. This disease is caused by mutation in gene coding collagene type X and has dominant inherited autosome. Radiologic image includes: widening and cupping of metatphyses, shortening of tubular bone genavara and coxavara. Ôn the basis of laboratory findings Ça, P and ÂLP are normal. Ïn other words, blood chemistry is normal. Ïn this study, report is given on a 13 months old neonate with Schmit type metaphyseal chonrodysplasia.
Full-Text [PDF 1863 kb]   (1850 Downloads)    
Type of Study: Research(Original) |

Add your comments about this article : Your username or Email:

© 2021 All Rights Reserved | Journal of Mazandaran University of Medical Sciences

Designed & Developed by : Yektaweb