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 (MRKH) syndrome

14 Mar 2007

Abstract excerpt

The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is characterized by congenital aplasia of the uterus and the upper part (2/3) of the vagina in women showing normal development of secondary sexual characteristics and a normal 46, XX karyotype. It affects at least 1 out of 4500 women. MRKH may be isolated (type I) but it is more frequently associated with renal, vertebral, and, to a lesser extent, auditory and...

Read the complete abstract on PubMed

Topics

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

Share to Gynecological conditions and treatments
Share to Sexual Differentiation and Disorders
Share to Urological Disorders and Treatments

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 17359527
DOI: 10.1186/1750-1172-2-13

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Mayer-Rokitansky-Küster-Hauser (MRKH) syndromePMID 17359527Read ↗

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

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

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

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

Genetics of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: advancements and implicationsSemantic proximity Read ↗

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

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

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

The Embryological Landscape of Mayer-Rokitansky-Kuster-Hauser Syndrome: Genetics and Environmental Factors.Semantic proximity Read ↗

Endometrial organoids derived from Mayer–Rokitansky–Küster–Hauser syndrome patients provide insights into disease-causing pathwaysSemantic proximity Read ↗

Surrogate in vitro fertilization outcome in typical and atypical forms of Mayer-Rokitansky-Kuster-Hauser syndromeSemantic proximity Read ↗

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