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

46,XY pure gonadal dysgenesis (Swyer-James syndrome)--Y or Y not?: a review.

Obstetrical & gynecological survey - 1 Feb 1994

Guidozzi F, Ball J, Spurdle A

Abstract excerpt

The designation "pure gonadal dysgenesis" is applied to a particular variety of defective organo-genesis, in which phenotypically female patients with a 46,XY karyotype have complete lack of functioning gonadal tissue. The latter are represented anatomically by the presence of bilateral, elongated, nonfunctioning, rudimentary "streak" gonads composed of fibrous tissue, although normal female internal genitalia...

Topics

Adult
DNA
Female
Gonadal Dysgenesis, 46,XY
Humans
Phenotype
Polymerase Chain Reaction
Sex Determination Analysis

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 8164912
DOI: 10.1097/00006254-199402000-00026

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 29 Aug 2026. Prepared record publication-8164912-2026-08-29.1. Manifest publication-graph-cohort-2026-08-29.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 29 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

46,XY pure gonadal dysgenesis (Swyer-James syndrome)--Y or Y not?: a review.PMID 8164912Read ↗

[Pure 46,XY gonadal dysgenesis].Semantic proximity Read ↗

Rare SRY-negative 46,XX disorder of sex development with male phenotype and ectopic gonads: a case report.Semantic proximity Read ↗

Swyer syndromeSemantic proximity Read ↗

[Pure 46XY gonadal dysgenesis].Semantic proximity Read ↗

Dysgerminoma in a case of 46, XY pure gonadal dysgenesis (Swyer syndrome): a case report.Semantic proximity Read ↗

Complete gonadal dysgenesis 46,XY (Swyer syndrome) in two sisters and their mother's maternal aunt with a female phenotype.Semantic proximity Read ↗

The XY female and SWYER syndromeSemantic proximity Read ↗

Fertility and pregnancy issues in a 46, XY (Swyer syndrome) patient in the face of ovarian cancerSemantic proximity Read ↗

A rare case of Swyer syndrome from Pakistan in a young girl with primary amenorrhea and 46XY genotype.Semantic proximity Read ↗

Management of 46, XY partial gonadal dysgenesis--revisited.Semantic proximity Read ↗

A case report of an incidental finding of a 46,XX, SRY-negative male with masculine phenotype during standard fertility workup with review of the literature and proposed immediate and long-term management guidance.Semantic proximity Read ↗

Embryological–clinical classification of female genital tract malformations – a review and updateSemantic proximity Read ↗

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