A REPORT OF A RARE CASE OF ACHONDROGENESIS SYNDROM TYPE II

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BOSKABADI H.; MAMOURI GH.A.

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Journal Paper

Paper Information

Journal: Iranian Journal of Obstetrics, Gynecology and Infertility Year:2008 | Volume:11 | Issue:2 Page(s): 61-64

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Information Journal Paper

Title

A REPORT OF A RARE CASE OF ACHONDROGENESIS SYNDROM TYPE II

Author(s)

BOSKABADI H. | MAMOURI GH.A. | Issue Writer Certificate

Keywords

ACHONDROGESISQ3

HYDROPSEQ3

CHONDRODYSTHROPHYQ2

Abstract

Introduction: ACHONDROGESIS is a rare severs skeletal displasia. Clinical findings include large head, small narrow thorax, extreme limb shortening, variable degree of hydrops fetalis. Most babies die in uterus.Case Report: In this article a rare case of this disease (type II) with all of clinical findings, and characteristics radiological features (short limb, large head, skeletal deformity, absence of ossification center of vertebra, pubis and sacrum is reponted.Conclusion: Antenatal diagnosis (villocentesis in the first trimesters and then experienced sonographer) and at birth clinical examination, radiographs, and autopsy are mandatory for making a specific diagnosis.

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APA: Copy

BOSKABADI, H., & MAMOURI, GH.A.. (2008). A REPORT OF A RARE CASE OF ACHONDROGENESIS SYNDROM TYPE II. IRANIAN JOURNAL OF OBSTETRICS, GYNECOLOGY AND INFERTILITY, 11(2), 61-64. SID. https://sid.ir/paper/65127/en

Vancouver: Copy

BOSKABADI H., MAMOURI GH.A.. A REPORT OF A RARE CASE OF ACHONDROGENESIS SYNDROM TYPE II. IRANIAN JOURNAL OF OBSTETRICS, GYNECOLOGY AND INFERTILITY[Internet]. 2008;11(2):61-64. Available from: https://sid.ir/paper/65127/en

IEEE: Copy

H. BOSKABADI, and GH.A. MAMOURI, “A REPORT OF A RARE CASE OF ACHONDROGENESIS SYNDROM TYPE II,” IRANIAN JOURNAL OF OBSTETRICS, GYNECOLOGY AND INFERTILITY, vol. 11, no. 2, pp. 61–64, 2008, [Online]. Available: https://sid.ir/paper/65127/en

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