Results 81 to 90 of about 3,002 (197)
PAX Genes in Cancer; Friends or Foes? [PDF]
, 2012 PAX genes have been shown to be critically required for the development of specific tissues and organs during embryogenesis. In addition, PAX genes are expressed in a handful of adult tissues where they are thought to play important roles, usually ...
Caiyun G. Li, Michael R. Eccles
core +1 more source
Clinical Endocrinology, Volume 104, Issue 2, Page 92-102, February 2026.ABSTRACT Background Mixed gonadal dysgenesis (MGD) is a rare form of differences in sex development (DSD) typically associated with 45,X/46,XY mosaicism. The phenotypic presentation of MGD varies from atypical genitalia to typical male or female appearances often associated with Turner stigmata.
Dinesh Giri +6 more
wiley +1 more source
AMH-RII : visió molecular de problemes hormonals en la diferenciació sexual [PDF]
, 2010 En l'esser humà, la sisena setmana del desenvolupament embrionari marca l'inici de la diferenciació dels conductes genitals. A l'embrió mascle, es genera una hormona que produeix la degeneració dels conductes de Müller (l'hormona anti-mülleriana AMH ...
Maréchal, Jean-Didier, Masgrau, Laura
core +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
Clinical Case Reports, Volume 14, Issue 1, January 2026.ABSTRACT Uterine didelphys, also known as double uterus, is a congenital anomaly of the female reproductive system that can be associated with a significant number of threatening obstetric complications, such as uterine rupture. We report a rare and complex case of an 18‐year‐old primigravida who presented with uterine rupture due to uterine didelphys ...
Asim Ali +7 more
wiley +1 more source
Immunohistochemical characterization of the anti-Müllerian hormone receptor type 2 (AMHR-2) in human testes [PDF]
, 2020 Purpose In males, AMH is secreted by immature Sertoli cells; following exposure to endogenous androgens, Sertoli cells undergo a process of maturation which ultimately inhibits AMH expression to undetectable levels in the serum.
Isidori A. M. +3 more
core +1 more source
Journal of Medical Case Reports, 2011 Introduction Persistent Mullerian duct syndrome is a rare form of male pseudo-hermaphroditism characterized by the presence of Mullerian duct structures in an otherwise phenotypically, as well as genotypically, normal man; only a few cases have been ...
Gujar Nishikant N +6 more
doaj +1 more source
Chronic Obstructive Uropathy Complicating Complete Androgen Insensitivity Syndrome: A Case Report
Case Reports in Endocrinology, Volume 2026, Issue 1, 2026.Complete androgen insensitivity syndrome (CAIS) is a rare X‐linked difference of sex development (DSD) caused by pathogenic variants in the androgen receptor (AR) gene, leading to complete androgen resistance. Diagnosis is often delayed in low‐resource settings due to a low index of suspicion and lack of access to diagnostic testing.
Brook Alemayehu Tesfaye +5 more
wiley +1 more source
Anogenital distance as a marker of androgen exposure in humans. [PDF]
, 2016 Abnormal foetal testis development has been proposed to underlie common disorders of the male reproductive system such as cryptorchidism, hypospadias, reduced semen quality and testicular germ cell tumour, which are regarded as components of a ...
Abbott +97 more
core +1 more source
PERSİSTENT MULLERIAN DUCT SYNDROME WITH TESTICULAR SEMINOMA
Urology Research and Practice, 2019 -
H. Hattat +3 more
doaj +2 more sources