Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

[Mayer-Rokitansky-Küster-Hauser syndrome. A report of two cases].

Ginecologia y obstetricia de Mexico - 1 Oct 2012

Bautista-Gómez Esperanza, Morales-García Víctor, Galván Espinosa Honorio, Flores-Romero Ana Luisa, Vásquez Santiago Edmundo, Pizarro Osorno Noel

Abstract excerpt

The Mayer-Rokitansky-Kuster-Hauser is a rare congenital anomaly characterized by lack of vaginal and uterine development variable and normal ovaries. It results from agenesis or hypoplasia Müller duct system. Cervicovaginal agenesis as part of the complex syndrome, is even rarer. We report two cases: adolescent patient with primary amenorrhea, cervicovaginal agenesis and chronic pelvic pain, and a 28-year-old...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to 46, XX Disorders of Sex Development
Share to Amenorrhea

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Hysterectomy

Share to Mullerian Ducts

Share to Somites

Share to Uterus

Share to Vagina

Source

Identifiers

PMID: 23240231

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Mayer-Rokitansky-Küster-Hauser syndrome. A report of two cases].PMID 23240231Read ↗

[The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: clinical description and genetics].Semantic proximity Read ↗

Phenotypic and clinical aspects of Mayer-Rokitansky-Küster-Hauser syndrome in a Chinese population: an analysis of 594 patients.Semantic proximity Read ↗

Mayer-Rokitansky-Küster-Hauser (MRKH) syndromeSemantic proximity Read ↗

Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: a comprehensive updateSemantic proximity Read ↗

Gonadal dysgenesis and the Mayer-Rokitansky-Kuster-Hauser Syndrome in a girl with a 46, XX karyotype: A case report and review of literatureSemantic proximity Read ↗

Genetics of Mayer–Rokitansky–Küster–Hauser ( MRKH ) syndromeSemantic proximity Read ↗

Familial occurrence of Mayer–Rokitansky–Küster–Hauser syndrome: A case report and review of the literatureSemantic proximity Read ↗

Mayer-Rokitansky-Kuster-Hauser Syndrome: Embryology, Genetics and Clinical and Surgical TreatmentSemantic proximity Read ↗

Clinical and genetic aspects of Mayer–Rokitansky–Küster–Hauser syndromeSemantic proximity Read ↗

The Mayer-Rokitansky-Küster-Hauser syndrome (congenital absence of uterus and vagina)--phenotypic manifestations and genetic approaches.Semantic proximity Read ↗

Rokitansky syndrome and MURCS association--clinical features and basis for diagnosis.Semantic proximity Read ↗

[The creation of a neovagina with laparoscopic technique].Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.