Evidence map›Paper›PMID 42803872›Full record

ReviewEndocrine2026

Growing up with Klinefelter syndrome: challenges of care in children and adolescents and patients advocacy.

Chiara Mameli, Maria Elisabeth Street, Mirta Vernice, Luigi Tarani, Camilla Valsecchi, Giulia Fiore, Cecilia Lugarà, Roberto Paparella, Anna Mariia Shulhai, Pamela Pedretti and 4 more

Abstract readReview
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In one paragraph

Review in Endocrine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Chiara MameliDepartment of Biomedical and Clinical Science, Università degli Studi di Milano, Milan, Italy. chiara.mameli@unimi.it.ORCID http://orcid.org/0000-0002-6768-3411
Maria Elisabeth StreetDepartment of Medicine and Surgery, University of Parma and Unit of Paediatrics University Hospital of Parma, Parma, Italy.
Mirta VerniceDepartment of Humanities (DISTUM), University of Urbino Carlo Bo, Urbino, Italy.
Luigi TaraniDepartment of Maternal Infantile and Urological Sciences, Sapienza University of Rome, Rome, Italy.
Camilla ValsecchiDepartment of Pediatrics, V.Buzzi Children's Hospital, Milan, Italy.
Giulia FioreDepartment of Health Sciences, Università degli Studi di Milano, Milan, Italy.
Cecilia LugaràDepartment of Human Pathology of Adulthood and Childhood, Unit of Pediatrics, University of Messina, Messina, Italy.
Roberto PaparellaDepartment of Maternal Infantile and Urological Sciences, Sapienza University of Rome, Rome, Italy.
Anna Mariia ShulhaiDepartment of Pediatrics, V.Buzzi Children's Hospital, Milan, Italy.
Pamela PedrettiAssociazione Nascere Klinefelter APS, Corinaldo, Italy.
Annapia VerriAssociazione Nascere Klinefelter APS, Corinaldo, Italy.
Elvira VerduciDepartment of Health Sciences, Università degli Studi di Milano, Milan, Italy.
Malgorzata WasniewskaDepartment of Human Pathology of Adulthood and Childhood, Unit of Pediatrics, University of Messina, Messina, Italy.
Tommaso AversaDepartment of Human Pathology of Adulthood and Childhood, Unit of Pediatrics, University of Messina, Messina, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Klinefelter syndrome (KS) is a common, yet underdiagnosed sex chromosome aneuploidy characterized by considerable phenotypic variability and multisystem involvement beginning in early life. The increasing use of noninvasive prenatal testing has led to earlier diagnosis, highlighting the need to redefine clinical management across the pediatric age. In this narrative review, pediatric endocrinologists, neuropsychiatrists, psychologists, and genetic experts critically examine current evidence on genetic mechanisms, growth, pubertal development, cardiometabolic risk, and neuropsychological features of KS, and includes a dedicated patient advocacy perspective highlighting family priorities and unmet needs. Emerging evidence indicates that altered body composition, insulin resistance, and neurodevelopmental vulnerabilities may arise in childhood, often preceding overt hypogonadism. Language impairment, executive dysfunction, and social cognitive difficulties represent key determinants of functional outcomes and require early recognition. Early childhood represents a window of opportunity for targeted interventions. A proactive, multidisciplinary, and preventive approach is essential to optimize long-term clinical, cognitive, and social outcomes in individuals with KS.

Indexed as

Klinefelter SyndromePatient AdvocacyAdolescentChildHumans

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.