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Title

Chromosomal Abnormalities Through Amniocentesis

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Abstract

 Objectives: The study aimed to assess the frequency and type of abnormal karyotype in Khuzestan, Iran by Amniocentesis before 22 weeks of gestation. Methods: We conducted a retrospective analysis of 1197 amniotic fluid specimens in Khuzestan province, before 22 weeks gestations for fetal karyotyping. Results: The incidence of abnormal aneuploidies was 4. 9% (59 of 1197) for all specimens. The highest chromosomal abnormality was Down Syndrome (64. 4%). Conclusions: The rate of Chromosomal Abnormalities was higher than other reports from Iran and all over the world. The detection rate of Down Syndrome similar to other reports remains high.

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    APA: Copy

    Pourahmad, Aghdas, SAADATI, NASRIN, BARATI, MOJGAN, MORAMEZI, FARIDEH, & MOHAMAD JAFARI, RAZIEH. (2019). Chromosomal Abnormalities Through Amniocentesis. JENTASHAPIR JOURNAL OF CELLULAR AND MOLECULAR BIOLOGY (JENTASHAPIR JOURNAL OF HEALTH RESEARCH), 10(2), 0-0. SID. https://sid.ir/paper/734683/en

    Vancouver: Copy

    Pourahmad Aghdas, SAADATI NASRIN, BARATI MOJGAN, MORAMEZI FARIDEH, MOHAMAD JAFARI RAZIEH. Chromosomal Abnormalities Through Amniocentesis. JENTASHAPIR JOURNAL OF CELLULAR AND MOLECULAR BIOLOGY (JENTASHAPIR JOURNAL OF HEALTH RESEARCH)[Internet]. 2019;10(2):0-0. Available from: https://sid.ir/paper/734683/en

    IEEE: Copy

    Aghdas Pourahmad, NASRIN SAADATI, MOJGAN BARATI, FARIDEH MORAMEZI, and RAZIEH MOHAMAD JAFARI, “Chromosomal Abnormalities Through Amniocentesis,” JENTASHAPIR JOURNAL OF CELLULAR AND MOLECULAR BIOLOGY (JENTASHAPIR JOURNAL OF HEALTH RESEARCH), vol. 10, no. 2, pp. 0–0, 2019, [Online]. Available: https://sid.ir/paper/734683/en

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