نتایج جستجو برای: mullerian anomalies

تعداد نتایج: 47956  

2013
Bushra Fiza Rati Mathur Pushpendra Saraswat

Keywords: Polycystic ovarian syndrome PCOS Anti-mullerian hormone AMH PCOD Original Article Polycystic ovarian syndrome is a complex heterogeneous disorder of unknown etiology and shows mild to severe degree of signs and symptoms affecting the reproductive, endocrine and metabolic functions. Anti-mullerian hormone, a dimeric glycoprotein belonging to the transforming growth factor–beta superfam...

2014
Brandon-Luke L. Seagle Keith J. Falter Stephen J. Lee Marina Frimer Robert Samuelson Shohreh Shahabi

•Two cases of large cervical mullerian adenosarcoma with sarcomatous overgrowth or heterologous elements and contrasting survival outcomes are reported.•When the diagnosis of mullerian adenosarcoma is uncertain or suspected, review of pathology by a national expert may be considered.•Rhabdomyoblastic differentiation of mullerian adenosarcoma may be a more aggressive histologic type.

2016
Sverre C. Christiansen Tina B. Eilertsen Eszter Vanky Sven M. Carlsen Wan-Xi Yang

CONTEXT Increased Anti-Mullerian Hormone in polycystic ovary syndrome, may be due to overactive follicles rather than reflect antral follicle count. OBJECTIVE Does Anti-Mullerian Hormone reflect antral follicle count similarly in women with or without polycystic ovary syndrome or polycystic ovarian morphology? DESIGN Cross-sectional, case-control. SETTING Women who delivered preterm in 19...

Journal: :journal of midwifery and reproductive health 0
behnaz souvizi assistant professor, department of obstetrics & gynecology, school of medicine, sabzevar university of medical sciences, sabzevar, iran reza jafarzadeh esfehani medical student, student research center, sabzevar university of medical sciences, sabzevar, iran

complete bicornuate uterus is a type of mullerian duct deformity, resulting from abnormal duct fusion. similar to other mullerian anomalies, bicornuate uterus is associated with specific complications during possible pregnancies. while various studies have reported successful deliveries in a bicornuate uterus, it might be accompanied with various complications, ranging from preterm labor to mor...

2014
Natarajan Suresh Shubhranshu Shekhar

Persistent Mullerian Duct Syndrome is a rare autosomal recessive disease characterized by persistent Mullerian derivative in patients with 46 XY Karyotype and normal virilization .Here we are presenting a case of incidental finding of Persistent Mullerian Duct Remnants in a 58 yr old man during routine hernioplasty.Histological diagnosis was confirmed by Immunohistochemistry

2018
Calvin Chao Vijay Vanguri Karl Uy

First described in 2005, the Mullerian derived cyst in the mediastinum is a rare finding with few subsequent reports. We report a case of Mullerian cyst occurring in the mediastinum of a 49-year-old female that was resected by robot-assisted thoracoscopic surgery. To our knowledge, this is the first report of robot-assisted resection of Hattori's cyst. Histopathologic analysis revealed ciliated...

Journal: :The International journal of developmental biology 2009
Yi Cai

Vaginal development has been a longstanding controversy, which hampers studies on vaginal diseases as well as cervical and uterine diseases. Most concerns center on: why is the vaginal epithelium different from the uterine epithelium; and where does the vagina originate from? It is commonly held that the rodent vagina has a dual origin: the cranial part is derived from the Mullerian duct (Mulle...

2015
Naila Parveen

OBJECTIVE: To compare the diagnostic accuracy of Anti-Mullerian hormone with follicle stimulating hormone for ovarian reserve assessment in infertile women by Receiver Operator Characteristic curve analysis. STUDY DESIGN: A Cross Sectional study. PLACE AND DURATION OF STUDY: At Institute of Basic Medical Sciences, University of Health Sciences in collaboration with nd th Gynecology and Obstetri...

Journal: :Journal of advances in medicine and medical research 2023

Introduction: Vaginal atresia is a component of Mayer–Rokitansky–Küster–Hauser syndrome (MRKHS), which includes variable Mullerian duct abnormalities with normal secondary sexual characteristics. Associated renal anomalies are present in about 30% cases(1)
 Objective: To rare variant MRKHS a14-y old female right ovary inguinal hernia and managed bysigmoid vaginoplasty.
 Case Descripti...

2014
Gayathri

The uterus is formed during embryogenesis by the fusion of the two paramesonephric ducts (also called mullerian ducts). This process usually fuses the two mullerian ducts into a single uterine body. Incomplete fusion of the mullerian ducts results in uterine malformation like uterus didelphus, uterus bicornis bicollis, uterus bicornis unicollis, uterus subseptate, uterus arcuate, and uterus uni...

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