Oviductal and uterine leiomyomata in mares [PDF]
, 2013 This paper describes a case of a sessile uterine leiomyoma in a 17-year-old chronic infertile Selle Francais mare. The mass was removed by transendoscopic electrocoagulation.
Chiers, Koen +5 more
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Classification conundrum: Persistent mullerian duct syndrome with hypospadias
Archives of Medicine and Health Sciences, 2016 The disorders of sex development (DSD) are uncommon and have wide phenotypic variation. Due to this, they often cannot be classified properly and go unreported.
Sheetal Arora, Ashish Kumar Mandal
doaj +1 more source
Insensibilidade androgênica completa e hérnia inguinal: relato de 3 casos. [PDF]
, 1999 Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina, Centro de Ciências da Saúde, Departamento de Pediatria, Curso de Medicina, Florianópolis ...
Queirós, Raquel Campos Galvão de
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PERSİSTENT MULLERIAN DUCT SYNDROME WITH TESTICULAR SEMINOMA
Urology Research and Practice, 2019 -
H. Hattat +3 more
doaj +2 more sources
Journal of Minimal Access Surgery, 2015 Persistent Mullerian duct syndrome (PMDS) is one of the three rare intersex disorders caused by defective anti-mullerian hormone or its receptor, characterized by undescended testes with presence of underdeveloped derivatives of mullerian duct in ...
Senthilnathan Palanisamy +5 more
doaj +1 more source
Functional characterization of a novel PBX1 de novo missense variant identified in a patient with syndromic congenital heart disease. [PDF]
, 2020 Pre-B cell leukemia factor 1 (PBX1) is an essential developmental transcription factor, mutations in which have recently been associated with CAKUTHED syndrome, characterized by multiple congenital defects including congenital heart disease (CHD). During
Alankarage, Dimuthu +9 more
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Indian Journal of Pathology and MicrobiologyPersistent Mullerian duct syndrome (PMDS) is a rare form of internal male pseudohermaphroditism in phenotypically males with 46 XY karyotype. The syndrome is caused by insufficient amount of Mullerian-inhibiting substance (MIS) or due to insensitivity of
Nibedita Sahoo +2 more
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Laparoscopic correction of transverse testicular ectopia with persistent Müllerian duct syndrome
Journal of Pediatric Surgery Case Reports, 2017 Transverse testicular ectopia (TTE) with persistent Müllerian duct syndrome (PMDS) is a rare genitourinary anomaly. Herein, we report a case of TTE with PMDS corrected laparoscopically.
Ji-Won Han, Chaeyoun Oh, Hyun-Young Kim
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A genomic atlas of human adrenal and gonad development [version 1; referees: awaiting peer review] [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 +9 more
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An extremely rare missense mutation of the androgen receptor gene in a Vietnamese family with complete androgen insensitivity syndrome [PDF]
, 2023 We report a Vietnamese family with complete androgen insensitivity syndrome that included several phenotypic females who have a 46,XY karyotype with an extremely rare mutation of the androgen receptor gene.
Ha, Thi Minh Thi +3 more
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