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

Endocrine and molecular investigations in a cohort of 25 adolescent males with prominent/persistent pubertal gynecomastia.

Andrology - 1 Mar 2016

Paris F, Gaspari L, Mbou F, Philibert P, Audran F, Morel Y, Biason-Lauber A, Sultan C

Abstract excerpt

Pubertal gynecomastia is a common condition observed in up to 65% of adolescent males. It is usually idiopathic and tends to regress within 1-2 years. In this descriptive cross-sectional study, we investigated 25 adolescent males with prominent (>B3) and/or persistent (>2 years) pubertal gynecomastia (P/PPG) to determine whether a hormonal/genetic defect might underline this condition. Endocrine investigation...

Read the complete abstract on PubMed

Topics

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

Share to Androgen-Insensitivity Syndrome
Share to Cohort Studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cross-Sectional Studies

Share to Gynecomastia

Share to Hormones

Share to Receptors, Androgen

Share to Steroid 17-alpha-Hydroxylase

Share to Transcriptome

Source

Identifiers

PMID: 26845730
DOI: 10.1111/andr.12145

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Endocrine and molecular investigations in a cohort of 25 adolescent males with prominent/persistent pubertal gynecomastia.PMID 26845730Read ↗

A rare cause of delayed puberty and primary amenorrhea: 17α-hydroxylase enzyme deficiency.Semantic proximity Read ↗

Aromatase excess syndrome: a rare autosomal dominant disorder leading to pre- or peri-pubertal onset gynecomastia.Semantic proximity Read ↗

A Rare Cause of Congenital Adrenal Hyperplasia: Clinical and Genetic Findings and Follow-up Characteristics of Six Patients with 17-Hydroxylase Deficiency Including Two Novel MutationsSemantic proximity Read ↗

Clinical review 148: Monogenic disorders of puberty.Semantic proximity Read ↗

Clinical management and genetic variation analysis of patients with 17β-hydroxysteroid dehydrogenase deficiency.Semantic proximity Read ↗

[Prepubertal gynecomastia at the debut of hereditary tumors predisposition syndrome (clinical case reports)].Semantic proximity Read ↗

3β-Hydroxysteroid dehydrogenase type-2 deficiency: Our experience and gonadal function-focused systematic review.Semantic proximity Read ↗

Genetic Insights into Prepubertal Gynecomastia: A Comprehensive Analysis of a Rare 45,X[2]/ 46,X, + mar[28] KaryotypeSemantic proximity Read ↗

Update on the etiology, diagnosis and therapeutic management of sexual precocity.Semantic proximity Read ↗

Pubertal presentation in seven patients with congenital adrenal hyperplasia due to P450 oxidoreductase deficiency.Semantic proximity Read ↗

A rare cause of delayed puberty in two cases with 46,XX and 46,XY karyotype: 17 α-hydroxylase deficiency due to a novel variant in CYP17A1 gene.Semantic proximity Read ↗

Taming Idiopathic Central Precocious Puberty: High Frequency of Imprinting Disorders in Familial Forms.Semantic proximity Read ↗

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