انوار, زهرا
مرکز تحقیقات ناباروری، دانشگاه علوم پزشکی شیراز، شیراز، ایران
[ 1 ] - بررسی ارتباط واریانت ژنتیکی UCP2 45bp ins/del با ناباروری آیدیوپاتیک در مردان
مقدمه: ناباروری یکی از مشکلات سلامت تولید مثل است که بسیاری از زوجین را در جهان تحت تاثیر قرار داده است و منجر به آسیب های روانی و عاطفـــی در زوجین می گردد. اعتقاد بر این هست که پروتئین های میتوکندریایی نقش مهمی در فرآیندهای ناباروری مردان دارند. یکی از مهم ترین این پروتئین ها UCP-2 می باشد که بیشتر از ده درصد پروتئین های غشای داخلی میتوکندری را تشکیل می دهد. هدف از این مطالعه بررسی ارتباط بین...
[ 2 ] - Genetic etiology of Asthenozoospermia: A review
Background: Asthenozoospermia, as the most prevalent cause of male infertility, is defined as low percentage of progressively motile spermatozoa per ejaculate. It occurs in both non-syndromic and syndromic forms and later it manifests as a part of primary ciliary dyskinesia. In the last decade, with the advent of Next-generation sequencing technologies numerous genes have been introduced in the...
[ 3 ] - Ovarian Hyperstimulation Syndrome: A Narrative Review of Its Pathophysiology, Risk Factors, Prevention, Classification, and Management
Ovarian hyperstimulation syndrome (OHSS) is a serious complication of ovulation induction that usually occurs after gonadotropin stimulation, followed by human chorionic gonadotropin administration, for infertility treatment. The existing knowledge about the pathophysiology, risk factors, and primary and secondary methods for the prevention of OHSS is reviewed in this manuscript. The clinical m...
[ 4 ] - Founder Effect of KHDC3L, p.M1V Mutation, on Iranian Patients with Recurrent Hydatidiform Moles
Background: Recurrent hydatidiform moles (RHMs) are an unusual pregnancy with at least two molar gestations that are associated with abnormal proliferation of trophoblastic tissue and a failure in the embryonic tissues development. Three maternal-effect genes, including NLRP7, KHDC3L, and PADI6 have been identified as the cause of RHMs. The present study aimed to understand the association of a...
[ 5 ] - A Novel Mutation in NLRP7 Related to Recurrent Hyda-tidiform Mole and Reproductive Failure
Objective Hydatidiform mole (HM) is an abnormal human pregnancy with excessive trophoblastic proliferation and abnormal embryonic development, which is divided into two Complete (CHM) and Partial (PHM) groups. One subcategory of the CHMs is recurrent and familial, which is known as biparental hydatidiform mole (BiHMs) or recurrent hydatidiform mole (RHM). NLRP7 and KHDC3L, two maternal-effect g...
[ 6 ] - Detection of Y Chromosome Microdeletions and Hormonal Profile Analysis of Infertile Men undergoing Assisted Reproductive Technologies
Objective Y chromosome deletions (YCDs) in azoospermia factor (AZF) region are associated with abnormal spermatogenesis and may lead to azoospermia or severe oligozoospermia. Assisted reproductive technologies (ART) by intracytoplasmic sperm injection (ICSI) and testicular sperm extraction (TESE) are commonly required for infertility management of patients carrying YCDs. The aim of this study w...
نویسندگان همکار