Results 11 to 20 of about 1,764,956 (149)

Persistent Mullerian Duct Syndrome with Polysplenia and Short Pancreas: A Case Report [PDF]

open access: yesJournal of Nepal Medical Association, 2019
Persistent Mullerian duct syndrome is a rare entity and usually presents with common symptoms of undescended testis and hernia. The syndrome is caused by an insufficient amount of Mullerian inhibiting substance or due to the insensitivity of the target ...
Umesh Kumar Sharma   +3 more
doaj   +4 more sources

Persistent mullerian duct syndrome

open access: yesIndian Journal of Radiology and Imaging, 2010
Persistent Mullerian duct syndrome (PMDS) is a rare form of internal male pseudohermaphroditism in which Mullerian duct derivatives are seen in a male patient. This syndrome is characterized by the persistence of Mullerian duct derivatives (i.e.
Divya Renu, B Ganesh Rao, K Ranganath
doaj   +5 more sources

Persistent Mullerian duct syndrome with polycystic ovary in a young adult: A rare case report [PDF]

open access: yesRadiology Case Reports, 2023
Persistent Mullerian Duct Syndrome (PMDS) is a type of pseudohermaphroditism that occurs in males. It is an autosomal recessive type of familial disease that is commonly associated with a history of consanguinity.
Awadia Gareeballah   +2 more
exaly   +3 more sources

Persistent Mullerian duct syndrome with testicular seminoma: A report of two cases

open access: yesIndian Journal of Urology, 2011
Persistent Mullerian duct syndrome is a rare form of male pseudohermaphroditism, characterized by the presence of the Mullerian duct structures in an otherwise phenotypically as well as genotypically normal male.
Renuka V Inuganti   +3 more
doaj   +2 more sources

Persistent mullerian duct syndrome in a patient with bilateral cryptorchid testes with seminoma

open access: yesJournal of Human Reproductive Sciences, 2012
Persistent mullerian duct syndrome (PMDS) is a rare form of male pseudohermaphroditism in which mullerian duct derivatives are present in an otherwise normally differentiated 46 XY male.
Shrinivasan Chamrajan   +3 more
doaj   +2 more sources

Female form of persistent mullerian duct syndrome: Rare entity

open access: yesUrology 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   +4 more
doaj   +2 more sources

Classification conundrum: Persistent mullerian duct syndrome with hypospadias

open access: yesArchives 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   +2 more sources

Persistent Mullerian Duct Syndrome in a Post Orchideopexy Patient with Gyanaecomastia and Hypospadias: A Case Report [PDF]

open access: yesJournal of Krishna Institute of Medical Sciences University, 2015
Persistent Mullerian Duct Syndrome (PMDS), a rare form of male pseudohermaphroditism. It is characterized by the persistence of Mullerian duct structures (uterus, fallopian tubes and upper two-thirds of vagina) in otherwise normally virilized males (
Vinay S. Kundargi   +5 more
doaj   +2 more sources

Persistent Mullerian Duct Syndrome: a rare entity with a rare presentation in need of multidisciplinary management

open access: yesInternational Brazilian Journal of Urology
Main findings: A typical male looking adolescent with a legal female gender assignment presented with haematuria. Investigations led to the diagnosis of Persistent Mullerian Duct Syndrome.
Lin Da Aw   +3 more
doaj   +2 more sources

Persistent mullerian duct syndrome with testicular seminoma in transverse testicular ectopia

open access: yesJournal of Human Reproductive Sciences, 2018
Persistent Mullerian Duct Syndrome (PMDS) is a disorder of male pseudohermaphroditism characterized by the persistence of Mullerian duct derivatives (uterus, fallopian tubes, and upper two-third of vagina) in a phenotypically and genotypically male ...
Sharada R Rane   +3 more
doaj   +2 more sources

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