Results 51 to 60 of about 2,744 (169)

Persistent Mullerian Duct Syndrome with Seminoma of Cryptorchid Testis: A Rare Case of Testicular Torsion Complication

Medical Journal of Dr. D.Y. Patil Vidyapeeth
Persistent Mullerian duct syndrome (PDMS) is characterized by the presence of Mullerian duct derivatives in a phenotypically and genetically normal individual. This is a case of a male in his 40s who was being evaluated for infertility.
Sikander Purohit, Anuradha C. K. Rao, Mary Mathew, Brij M. K. Singh   +3 more
doaj   +1 more source

Female form of persistent mullerian duct syndrome: Rare entity

Urology Annals, 2015
Persistent Mullerian duct syndrome (PMDS) is a rare form of Disorder of sex development in which Mullerian duct derivatives (fallopian tubes, uterus and the proximal vagina) are present in an otherwise normally differentiated 46 XY male.
Shailesh Solanki, Gowrishankar, Vinay Jadhav, M Narendra Babu, S Ramesh   +4 more
doaj   +1 more source

A novel member of the transmembrane serine/threonine kinase receptor family is specifically expressed in the gonads and in mesenchymal cells adjacent to the mullerian duct [PDF]

, 1994
The activin and TGF-beta type II receptors are members of a separate subfamily of transmembrane receptors with intrinsic protein kinase activity ...
Baarends, W.M. (Willy), Helmond, M.J. (Marjolein) van, Hoogerbrugge, J.W. (Jos), Karels, B. (Bas), Schoot, P.J.C.M. (Pieter) van der, Uilenbroek, J.Th.J. (Jan), Verhoef-Post, M. (Miriam), Winter, J.P. (Johan) de   +7 more
core  

Gendering the Menstrual Cycle in Behavioral Neuroendocrinology

American Journal of Human Biology, Volume 38, Issue 4, April 2026.
ABSTRACT The menstrual cycle is increasingly described as a “vital sign of the female body,” with the literature suggesting cycle‐related brain and behavioral changes. With growing interest in the effects that the menstrual cycle has on the brain, body and mind, characterizing what constitutes healthy cycle‐related change has become a central goal of ...
Annie Duchesne, Kiranjot Kaur Jhajj, Nicole White   +2 more
wiley   +1 more source

The Homeobox Genes: Classification, Regulation, Biological Functions, and Diseases

MedComm, Volume 7, Issue 4, April 2026.
Overview of the homeobox gene superfamily and its pathophysiological roles. The homeobox superfamily comprises several major classes, including ANTP, PRD, TALE, LIM, POU, and others. Among these, the HOX clusters (A–D) play critical roles in embryonic development specifically in conferring cellular identity, regulating morphogenesis, and guiding axial ...
Maedeh Dadzadi, Shahin Ramazi, Mona Darvazi, Sepideh Yoosefi, Melika Abbasi, Shirin Farsad   +5 more
wiley   +1 more source

Pathogenesis of Adenomyosis: An Integrated Review of Cellular Origins, Molecular Mechanisms, and Intersecting Diseases

Journal of Cellular and Molecular Medicine, Volume 30, Issue 7, April 2026.
ABSTRACT Adenomyosis is a prevalent disorder of the archimetra, historically conflated with endometriosis but possessing a unique pathobiological trajectory. This review synthesises current molecular evidence to propose a unified mechanistic framework initiated by tissue injury and repair (TIAR), aberrant stem cell activation, or de novo metaplasia ...
Jiang Yang, Xiaochong Li, Yu Peng, Zhongfeng Sun, Lingli Zhang, Jie Duan, Nanbert Zhong   +6 more
wiley   +1 more source

What Does AMH Tell Us in Pediatric Disorders of Sex Development? [PDF]

, 2020
Disorders of sex development (DSD) are conditions where genetic, gonadal and/or internal/external genital sex are discordant. In many cases, serum testosterone determination is insufficient for the differential diagnosis.
Josso, Nathalie, Rey, Rodolfo Alberto
core   +1 more source

Recurrent Constellations of Embryonic Malformations (RCEM): Teratogenicity Linked to Transient Hypoxia and Hormone Pregnancy Tests Agrees With RCEM and Suggest a Reactive Oxygen Species Pathogenesis

Birth Defects Research, Volume 118, Issue 3, March 2026.
ABSTRACT Background No consistent genetic etiology has been found for a group of six different conditions in humans with multiple malformations called “recurrent constellations of embryonic malformations” (RCEM). Recent studies indicate hypoxia/reoxygenation and generation Reactive Oxygen Species (ROS) as an underlying mechanism for RCEM with the ...
Aaron P. Adam, Helen E. Ritchie, Margaret P. Adam, Bengt R. Danielsson   +3 more
wiley   +1 more source

A genomic atlas of human adrenal and gonad development [version 2; referees: 4 approved] [PDF]

, 2017
BACKGROUND: In humans, the adrenal glands and gonads undergo distinct biological events between 6-10 weeks post conception (wpc), such as testis determination, the onset of steroidogenesis and primordial germ cell development.
Achermann, JC, Barenco, M, Buonocore, F, del Valle, I, Duncan, AJ, Gerrelli, D, Hubank, M, Lin, L, Parnaik, R, Shah, S   +9 more
core   +4 more sources

AMHR2 mutation in persistent Müllerian duct syndrome: A case of transverse testicular ectopia

UroPrecision, Volume 4, Issue 1, Page 64-68, March 2026.
Abstract Backgroud Persistent Müllerian duct syndrome (PMDS) is a rare condition characterized by the persistence of Müllerian duct structures in genotypic and phenotypic males. Case Presentation We present the case of a 4‐month‐old male with PMDS who presented with transverse testicular ectopia. The patient underwent diagnostic laparoscopic orchiopexy
Hangcheng Fu, Weijing Huang, Jeffrey T. White   +2 more
wiley   +1 more source