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Article

Three new 46,XX male patients: a clinical, cytogenetic and molecular analysis.

Journal of pediatric endocrinology & metabolism : JPEM - 1 Feb 2005

Grigorescu-Sido Anca, Heinrich Udo, Grigorescu-Sido Paula, Jauch Anna, Hager Hans-Dieter, Vogt Peter H, Duncea Ileana, Bettendorf Markus

Abstract excerpt

BACKGROUND: XX males range phenotypically from completely masculinised individuals to true hermaphrodites and include a subset of SRY negative patients. The correlation between genotype (SRY+/-) and phenotype is still unclear. AIM: To report three new patients with this rare condition, one of whom was diagnosed prenatally and another was SRY negative, and to verify in our patients whether the presence of SRY...

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Topics

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Share to Chromosomes, Human, X
Share to Disorders of Sex Development

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

Share to Dosage Compensation, Genetic

Share to Karyotyping

Share to Nuclear Proteins

Share to Sex-Determining Region Y Protein

Share to Translocation, Genetic

Share to Virilism

Source

Identifiers

PMID: 15751609
DOI: 10.1515/jpem.2005.18.2.197

Genes

SRY

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.

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