کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
8695252 | 1581971 | 2018 | 8 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Screening chromosomal anomalies in early pregnancy: When and why
ترجمه فارسی عنوان
غربالگری ناهنجاری های کروموزومی در اوایل بارداری: وقتی و چرا
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کلمات کلیدی
موضوعات مرتبط
علوم پزشکی و سلامت
پزشکی و دندانپزشکی
مراقبت های ویژه و مراقبتهای ویژه پزشکی
چکیده انگلیسی
Prenatal screening for aneuploidies is done using maternal serum and sonographic markers. Although many screening tests are available, their correct application still does not have uniformity. This review will give insight into the existing screening protocols, their merits and demerits, interpretation of results and the relevance of these tests in low resource settings. Cell free fetal DNA and its exciting role in non invasive prenatal testing along with its advantages and drawbacks is also taken up. We have further considered the role of counseling and its importance before embarking on the screening tests. The upcoming role of maternal serum markers for prediction of adverse obstetrical outcomes is also discussed.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Indian Journal of Medical Specialities - Volume 9, Issue 2, AprilâJune 2018, Pages 86-93
Journal: Indian Journal of Medical Specialities - Volume 9, Issue 2, AprilâJune 2018, Pages 86-93
نویسندگان
Ayesha Ahmad, Aruna Nigam, Saloni Arora, Smriti Prasad,