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

The Persistent Müllerian Duct Syndrome: An Update Based Upon a Personal Experience of 157 Cases.

Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation - 1 Jan 2017

Picard Jean-Yves, Cate Richard L, Racine Chrystèle, Josso Nathalie

Abstract excerpt

Male sex differentiation is driven by 2 hormones, testosterone and anti-müllerian hormone (AMH), responsible for the regression of müllerian ducts in male fetuses. Mutations inactivating AMH or its receptor AMHRII lead to the persistent müllerian duct syndrome (PMDS) in otherwise normally virilized 46,XY males. Our objective was to review the clinical, anatomical, and molecular features of PMDS based upon a...

Read the complete abstract on PubMed

Topics

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

Share to Anti-Mullerian Hormone
Share to Disorder of Sex Development, 46,XY

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

Share to AMH gene

Share to Hormones

Share to Inheritance Patterns

Share to Models, Molecular

Share to Mutation

Share to Sexual Differentiation and Disorders

Source

Identifiers

PMID: 28528332
DOI: 10.1159/000475516

Genes

AMH

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

The Persistent Müllerian Duct Syndrome: An Update Based Upon a Personal Experience of 157 Cases.PMID 28528332Read ↗

Persistent Müllerian duct syndrome: an update.Semantic proximity Read ↗

Persistent Müllerian Duct Syndrome Caused by a Novel Mutation of an Anti-MüIlerian Hormone Receptor Gene: Case Presentation and Literature Review.Semantic proximity Read ↗

A Surgical and Clinical Approach to Persistent Müllerian Duct Syndrome: Laparoscopic, Histological, and Molecular Findings.Semantic proximity Read ↗

Persistent Mï¿½llerian duct syndrome: A case report and reviewSemantic proximity Read ↗

Novel AMH and AMHR2 Mutations in Two Egyptian Families with Persistent Müllerian Duct Syndrome.Semantic proximity Read ↗

A Novel Mutation of AMHR2 in Two Siblings with Persistent Müllerian Duct SyndromeSemantic proximity Read ↗

Identification of AMH and AMHR2 Variants Led to the Diagnosis of Persistent Müllerian Duct Syndrome in Three Cases.Semantic proximity Read ↗

AMH and AMHR2 Involvement in Congenital Disorders of Sex DevelopmentSemantic proximity Read ↗

AMH and AMH receptor defects in persistent Müllerian duct syndromeSemantic proximity Read ↗

A novel mutation of AMHR2 in two brothers with persistent Müllerian duct syndrome and their intracytoplasmic sperm injection outcome.Semantic proximity Read ↗

Identification of four novel variant in the AMHR2 gene in six unrelated Turkish families.Semantic proximity Read ↗

Management and Molecular Diagnosis of Persistent Müllerian Duct Syndrome in Chinese PatientsSemantic proximity Read ↗

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