Results 81 to 90 of about 1,764,956 (149)

PERSISTENT MULLERIAN DUCT SYNDROME AND TRANSVERSE TESTICULAR ECTOPIA

open access: yesUrology Research and Practice, 2019
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Muzaffer EROĞLU   +2 more
doaj   +2 more sources

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

A Novel Mutation of AMHR2 In Two Siblings with Persistent Mullerian Duct Syndrome

open access: yes, 2017
Persistent mullerian duct syndrome (PMDS) is characterized by the presence of mullerian duct derivatives in otherwise phenotypically normal males. It is caused in approximately 85% of the cases by mutations in the AMH gene or its type II receptor (AMHR2).
Haluk Emir   +15 more
core   +1 more source

Laparoscopic correction of transverse testicular ectopia with persistent Müllerian duct syndrome

open access: yesJournal 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
doaj   +1 more source

Persistent Mullerian duct syndrome: A case report and review of the literature

open access: yes, 2011
Persistent Mullerian duct syndrome is a rare form of internal male pseudohermaphroditism, in which Mullerian duct derivatives (uterus and fallopian tubes) are present in a genotypic (46XY) and phenotypic male.
Nasir, AA, Odi, TO, Abdur-Rahman, LO
core   +1 more source

An insight into the landscape of a rare tumor-persistent Mullerian duct syndrome with testicular seminoma

open access: yesIndian Journal of Pathology and Microbiology
Persistent 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
doaj   +1 more source

Transverse testicular ectopia and persistent Mullerian duct syndrome: video-assisted treatment

open access: yes, 2010
Persistent Mullerian duct syndrome (PMDS) is a rare autosomal recessive disorder in which, due to a deficiency of the Mullerian inhibiting substance (MIS), the complete development of the Mullerian duct structures occurs in the presence of a male ...
GARGANO, TOMMASO   +5 more
core   +1 more source

A rare cause of a 46, XY disorders of sex development: Persistent mullerian duct syndrome

open access: yes, 2017
Persistent mullerian duct syndrome (PMDS) is a relatively rare form of a 46, XY disorders of sex development and clinically characterized by undescended testes and the presence of mullerian duct derivatives such as a uterus and fallopian tubes in males ...
Sezer Acar   +13 more
core   +1 more source

Autosomal recessive segregation of a truncating mutation of anti-Mullerian type II receptor in a family affected by the persistent Mullerian duct syndrome contrasts with its dominant negative activity in vitro.

open access: yes, 2001
peer reviewedAnti-Mullerian hormone belongs to the TGFbeta family whose members exert their effects by signaling through two related serine/threonine kinase receptors.
Belville, C.   +9 more
core   +1 more source

Persistent Müllerian duct syndrome: a rare clinical image. [PDF]

open access: yesPan Afr Med J, 2023
Maheswara Y, Meshram R.
europepmc   +1 more source

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