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

Long term outcome in adult males with classic congenital adrenal hyperplasia.

The Journal of clinical endocrinology and metabolism - 1 Jul 2001

Cabrera M S, Vogiatzi M G, New M I

Abstract excerpt

The effects of classic congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency on final height and fertility were evaluated in 30 affected males, aged 17-43 yr. The mean adult height of these patients was 165.64 +/- 8.4 cm (mean +/- SD), with a mean SD score of -1.65 +/- 1.2 cm. The difference between the mean final height SD score and mean target height SD score was -1.67 +/- 1.0 cm. All patients...

Read the complete abstract on PubMed

Topics

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

Share to Leydig Cells
Share to Adrenal Hyperplasia, Congenital
Share to Body Height

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Follicle Stimulating Hormone

Share to Gonadotropin-Releasing Hormone

Share to Luteinizing Hormone

Share to Oligospermia

Source

Identifiers

PMID: 11443169
DOI: 10.1210/jcem.86.7.7668

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

Long term outcome in adult males with classic congenital adrenal hyperplasia.PMID 11443169Read ↗

Semen quality and testicular adrenal rest tumour development in 46,XY congenital adrenal hyperplasia: the importance of optimal hormonal replacement.Semantic proximity Read ↗

Diagnosis and management of classical congenital adrenal hyperplasia.Semantic proximity Read ↗

Final height in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: the Italian experience.Semantic proximity Read ↗

Clinical perspectives in congenital adrenal hyperplasia due to 3β-hydroxysteroid dehydrogenase type 2 deficiencySemantic proximity Read ↗

Congenital adrenal hyperplasia clinical characteristics and genotype in newborn, childhood and adolescence.Semantic proximity Read ↗

Congenital Adrenal Hyperplasia.Semantic proximity Read ↗

Gonadal function in adult male patients with congenital adrenal hyperplasiaSemantic proximity Read ↗

Follow-Up of 68 Children with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency: Relevance of Genotype for ManagementSemantic proximity Read ↗

Non-Classical Congenital Adrenal Hyperplasia in Childhood.Semantic proximity Read ↗

[Health status of adults with congenital adrenal hyperplasia due to 21-hydroxylase deficiency].Semantic proximity Read ↗

Fractures and bone mineral density in adult women with 21-hydroxylase deficiency.Semantic proximity Read ↗

Extensive clinical experience: nonclassical 21-hydroxylase deficiency.Semantic proximity Read ↗

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