ReviewEuropean journal of pediatrics2025
Beyond endocrine features in non-classical congenital adrenal hyperplasia: a narrative review of psychoneuro-social perspectives in pediatric and adolescent patients.
Review in European journal of pediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
3 citing papers in PubMed.
- Trajectory-based analysis of growth in congenital adrenal hyperplasia: therapeutic implications for final height preservation.European journal of pediatrics · 2026Observational
- Early Risk Stratification in Non-Classical Congenital Adrenal Hyperplasia Based on Newborn 17-OHP Screening Values, Hormonal Findings, and Genotype.Journal of clinical medicine · 2026Article
- Case Report: Compound heterozygous mutation comprising p.Pro31Leu and exons 1-3 ins/del variants inFrontiers in pediatrics · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
9 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Non-classical congenital adrenal hyperplasia (NCCAH) is a late-onset, milder form of 21-hydroxylase deficiency marked by adrenal androgen excess. While endocrine aspects are well described, psychoneuro-social outcomes in pediatric and adolescent patients remain less clearly defined. A literature search of MEDLINE (PubMed) was conducted in July 2025 using "Non-Classical Congenital Adrenal Hyperplasia" with terms related to mental health, cognition, social adaptation, gender identity, sexual orientation, and heterozygous carriers. In females, androgen excess is frequently associated with anxiety, depression, body image concerns, and increased prevalence of gender nonconformity or non-heterosexual orientation, although most maintain a female gender identity. Males generally present fewer gender identity concerns, with inconsistent evidence for higher externalizing behaviors. Neurocognitive outcomes are variable, with occasional subtle deficits in working memory, executive function, or attention, alongside possible strengths in visuospatial tasks. Health-related quality of life in adequately treated pediatric NCCAH is generally comparable to that of healthy peers, though age-specific psychosocial vulnerabilities may occur. Social difficulties, particularly among females, may involve stigmatization and reduced peer acceptance. Heterozygous CYP21A2 carriers are usually asymptomatic and do not exhibit significant psychoneuro-social burden; interventions are not routinely indicated unless hyperandrogenic symptoms are present.
conclusionsPsychoneuro-social effects of NCCAH are heterogeneous and shaped by sex, age, and clinical presentation. An individualized, multidisciplinary approach integrating endocrinology, psychological support, and social resources is recommended. Longitudinal studies are needed to clarify long-term trajectories and optimize targeted interventions. WHAT IS KNOWN: • NCCAH is a common form of CAH with mild androgen excess. • Its endocrine features are well described, but psychosocial aspects are often overlooked. WHAT IS NEW: • This review highlights cognitive, emotional, and social challenges in pediatric NCCAH. • Sex-specific patterns and the role of early diagnosis in improving outcomes are emphasized.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.