Results 71 to 80 of about 647,943 (150)

Unilateral ductus deferens aplasia with terminal cystic dilation in a Bernese mountain dog

open access: yesVeterinary Record Case Reports, Volume 14, Issue 3, August 2026.
Abstract An incidental caudal abdominal mass was discovered in a 5‐year‐old, male, entire Bernese mountain dog. Investigations showed a terminal cystic dilation of the left ductus deferens. Castration, along with surgical resection of the mass, was performed, and histopathology of the mass and ductus deferens was consistent with segmental aplasia of ...
Daisy Johnson   +3 more
wiley   +1 more source

Persistent Mullerian duct syndrome with seminoma: report of a case

open access: yes, 1985
Persistent Mullerian duct syndrome is a male hermaphroditism in which remnants of Mullerian ducts occur from abnormality of Mullerian inhibitory factor and often cause transverse testicular ectopia or hernia uteri inguinalis.
若林, 昭   +5 more
core  

Persistent mullerian duct syndrome with seminoma: report of a case [PDF]

open access: yes, 1992
22歳男, 交叉性精巣偏位に精巣腫瘍を合併した例としては, 本邦16例目である.さらに自験例の右胸水貯留は, Meigs症候群と同様の機序が考えられたA case of persistent Mullerian duct syndrome associated with seminoma is reported. A 22-year-old man was admitted with the chief complaint of left flank colicky pain.
西岡, 伯   +3 more
core  

Persistent Mullerian Duct Syndrome (PMDS) Presenting as a Malignant Tumour

open access: yes, 2018
Persistent Mullerian duct syndrome is a condition in which there is presence of Mullerian duct structures (uterus, fallopian tube, vagina etc.) in an otherwise phenotypically, as well as genotypically, normal man.
Md Rafiqul Islam   +2 more
core   +1 more source

Carcinoma in third testis in a case of polyorchidism and persistent mullerian structure syndrome : A case report and review of literature

open access: yesIndian Journal of Urology, 2002
Polyorchidism is a rare but distinct genital anomaly in which supernumerary testes are present usually within the scrotum. A unique case of germ cell tumour arising in one of the two cryptorchid abdominal testes with persistent mullerian structure ...
S Kumar   +3 more
doaj  

Male form of persistent Mullerian duct syndrome type I (hernia uteri inguinalis) presenting as an obstructed inguinal hernia: a case report

open access: yesJournal 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

Persistent Mullerian duct syndrome: A novel mutation in the Anti-Mullerian Hormone gene

open access: yes, 2017
BACKGROUND AND OBJECTIVE: Persistent Mullerian duct syndrome (PMDS) is a relatively rare form of 46, XY disorder of sex development caused by the failure of formation, release or action of anti-Mullerian hormone (AMH) in intrauterine life. In this report
Onay H.   +5 more
core   +1 more source

Two heterozygous mutations of the AMH gene in a Japanese patient with persistent Mullerian duct syndrome [PDF]

open access: yes, 2014
Persistent Mullerian duct syndrome (PMDS) is an autosomal recessive disorder of sex development (DSD) characterized by the presence of Mullerian duct derivatives in 46, XY phenotypic males.
Ishizu, Katsura   +3 more
core   +1 more source

US and MRI in a case of persistent Mullerian duct syndrome

open access: yes, 1998
We report the US and MR appearances in a case of persistent Mullerian duct syndrome, a rare form of inherited male pseudohermaphroditism characterised by the presence of uterus and fallopian tubes in a normally virilised 46XY ...
DI CESARE, Ernesto   +4 more
core   +1 more source

Persistent Mullerian duct syndrome: the hidden normal or abnormal anatomy and the value of laparoscopy [PDF]

open access: yes, 2015
Persistent Mullerian duct syndrome (PMDS) is a rare disorder of male sexual development. It is characterized by the presence of a uterus, fallopian tubes, and upper vagina in an otherwise phenotypically and genotypically normal male. This malformation is
Parida, L, Alwabari, A, Al-Salem, AH
core   +1 more source

Home - About - Disclaimer - Privacy