CASE REPORT ON SCHMID TYPE METAPHYSEAL CHONDRODYSPLASIA

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HAYDARYAN F.

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Journal Paper

Paper Information

Journal: JOURNAL OF MAZANDARAN UNIVERSITY OF MEDICAL SCIENCES Year:2003 | Volume:13 | Issue:38 Page(s): 81-84

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Information Journal Paper

Title

CASE REPORT ON SCHMID TYPE METAPHYSEAL CHONDRODYSPLASIA

Author(s)

HAYDARYAN F. | Issue Writer Certificate

Keywords

DWARFISMQ3

CHONDRODYSPLASIAQ4

ECTROMELIAQ4

Abstract

Mataphyseal CHONDRODYSPLASIA is a term for group of dysplasias, characterized by radiographic changes in metaphyse tubular bones with normal epiphysis. It 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. On the basis of laboratory findings Ca, P and ALP are normal. In other words, blood chemistry is normal. In this study, report is given on a 13 months old neonate with Schmit type metaphyseal chonrodysplasia.

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APA: Copy

HAYDARYAN, F.. (2003). CASE REPORT ON SCHMID TYPE METAPHYSEAL CHONDRODYSPLASIA. JOURNAL OF MAZANDARAN UNIVERSITY OF MEDICAL SCIENCES, 13(38), 81-84. SID. https://sid.ir/paper/44766/en

Vancouver: Copy

HAYDARYAN F.. CASE REPORT ON SCHMID TYPE METAPHYSEAL CHONDRODYSPLASIA. JOURNAL OF MAZANDARAN UNIVERSITY OF MEDICAL SCIENCES[Internet]. 2003;13(38):81-84. Available from: https://sid.ir/paper/44766/en

IEEE: Copy

F. HAYDARYAN, “CASE REPORT ON SCHMID TYPE METAPHYSEAL CHONDRODYSPLASIA,” JOURNAL OF MAZANDARAN UNIVERSITY OF MEDICAL SCIENCES, vol. 13, no. 38, pp. 81–84, 2003, [Online]. Available: https://sid.ir/paper/44766/en

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