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

Genotype, Mortality, Morbidity, and Outcomes of 3β-Hydroxysteroid Dehydrogenase Deficiency in Algeria.

Frontiers in endocrinology - 1 Jan 2022

Ladjouze Asmahane, Donaldson Malcolm, Plotton Ingrid, Djenane Nacima, Mohammedi Kahina, Tardy-Guidollet Véronique, Mallet Delphine, Boulesnane Kamélia, Bouzerar Zair, Morel Yves, Roucher-Boulez Florence

Abstract excerpt

Background: 3β-hydroxysteroid dehydrogenase 2 (3βHSD2) deficiency is a rare form of congenital adrenal hyperplasia (CAH), with fewer than 200 cases reported in the world literature and few data on outcomes. Patients and Methods: We report a mixed longitudinal and cross-sectional study from a single Algerian center between 2007 and 2021. Virilization and under-masculinization were assessed using Prader staging and...

Read the complete abstract on PubMed

Topics

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

Share to Adrenal Gland Neoplasms
Share to Adrenal Hyperplasia, Congenital

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Algeria

Share to Chromatography, Liquid

Share to Cross-Sectional Studies

Share to Morbidity

Share to Polycystic Ovary Syndrome

Share to Tandem Mass Spectrometry

Source

Open in PubMed Open full text

Identifiers

PMID: 35757411
DOI: 10.3389/fendo.2022.867073
PMCID: PMC9229600

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

Genotype, Mortality, Morbidity, and Outcomes of 3β-Hydroxysteroid Dehydrogenase Deficiency in Algeria.PMID 35757411Read ↗

Revisiting Classical 3β-hydroxysteroid Dehydrogenase 2 Deficiency: Lessons from 31 Pediatric CasesSemantic proximity Read ↗

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

Congenital adrenal hyperplasia in Saudi Arabia: Epidemiology, genetic mutations, and evolving management strategies.Semantic proximity Read ↗

Single-Center Experience in Five Patients Diagnosed with Lipoid Congenital Adrenal Hyperplasia due to Steroidogenic Acute Regulatory Protein (STAR) Gene Variants: A Rare Cause of Adrenal InsufficiencySemantic proximity Read ↗

The next 150 years of congenital adrenal hyperplasia.Semantic proximity Read ↗

Non-classical 11β-hydroxylase deficiency caused by a novel heterozygous mutation: a case report and review of the literature.Semantic proximity Read ↗

Genotype-Phenotype Correlation and Feminizing Surgery in Danish Children with Congenital Adrenal Hyperplasia.Semantic proximity Read ↗

[Clinical and StAR genetic characteristics of 33 children with congenital lipoid adrenal hyperplasia].Semantic proximity Read ↗

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

Ethnic and National Differences in Congenital Adrenal Hyperplasia Incidence: A Systematic Review and Meta-Analysis.Semantic proximity Read ↗

Rare forms of congenital adrenal hyperplasia: pathogenesis, clinical, treatment and management.Semantic proximity Read ↗

Congenital Adrenal Hyperplasia-Current Insights in Pathophysiology, Diagnostics, and Management.Semantic proximity Read ↗

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