Evidence map›Paper›PMID 40842493›Full record

ReviewFrontiers in endocrinology2025

The clinical approach to child and adolescent patients with lipodystrophy: a series of international case discussions.

Rebecca J Brown, Baris Akinci, Saif Al Yaarubi, Elise Bismuth, Marco Cappa, Asma Deeb, Clemens Kamrath, Carla Musso, Nivedita Patni, Flavia Prodam and 2 more

Abstract readCase ReportsReview
In one paragraph

Review in Frontiers in endocrinology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Hematopoietic stem cell transplantation-associated partial lipodystrophy.Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology · 2026
    Review
  3. Article
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

12 authors.

Rebecca J BrownNational Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD, United States.
Baris AkinciDepartment of Technological Research, Izmir Biomedicine and Genome Center, Dokuz Eylül University, Izmir, Türkiye.
Saif Al YaarubiOman Medical Specialty Board, Muscat, Oman.
Elise BismuthDepartment of Pediatric Endocrinology, Assistance Publique-Hôpitaux de Paris, Robert Debré Hospital, Paris, France.
Marco CappaResearch Unit for Innovative Therapies in Endocrinopathies, Bambino Gesù Children's Hospital, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Rome, Italy.
Asma DeebDivision of Paediatric Endocrine, Sheikh Shakhbout Medical City and College of Medicine and Health Sciences, Khalifa University, Abu Dhabi, United Arab Emirates.
Clemens KamrathCentre of Child and Adolescent Medicine, Department of General Pediatrics and Neonatology, University Hospital Freiburg, Freiburg, Germany.
Carla MussoHospital Universitario Fundación Favaloro, Ciudad Autónoma de Buenos Aires, Argentina.
Nivedita PatniDivision of Pediatric Endocrinology, Department of Pediatrics, University of Texas (UT) Southwestern Medical Center, Dallas, TX, United States.
Flavia ProdamUnit of Endocrinology, Department of Health Sciences, University of Eastern Piedmont, Novara, Italy.
Rachel WilliamsCambridge University Hospitals, National Health Service (NHS) Foundation Trust, Cambridge, United Kingdom.
Martin WabitschGerman Center for Child and Adolescent Health (DZKJ), Ulm Site, Division of Pediatric Endocrinology and Diabetes, Department of Pediatrics and Adolescent Medicine, University Medical Center, Ulm, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Lipodystrophy syndromes comprise a group of rare endocrine disorders characterized by the generalized or partial loss of adipose tissue. Affected individuals frequently display absolute or relative reductions in leptin, a key adipokine regulator of hunger-satiety signaling, and are predisposed to a range of metabolic and end-organ complications, often from a young age. The presentation and severity of lipodystrophy syndromes is largely dependent on the extent of adipose tissue loss while comorbidities often deteriorate with age. In this regard, optimizing care for children and adolescents with lipodystrophy syndromes is a pivotal step in supporting them into adulthood. To assist clinicians with limited experience of managing young patients with lipodystrophy syndromes, we describe our clinical approach to a series of pediatric patients with these rare diseases. Methods: The clinical history, diagnosis, disease management and follow-up care of 10 international pediatric patients with lipodystrophy syndromes are presented. Teaching points from each case study are also provided. Most of these cases are based on patients from our clinics with certain details changed to protect privacy. Others represent hypothetical scenarios based on our clinical experience supported by review of the medical literature and are included here for educational purposes. Results: Our patients illustrate the broad phenotypic spectrum of lipodystrophy syndromes that can manifest early in life. We highlight the importance of timely and accurate diagnosis in guiding early disease management strategies to help reduce the risk of comorbidities. The challenges faced by clinicians managing pediatric patients with lipodystrophy syndromes and how these challenges may differ from adult patients are also explored. Discussion: The cases presented in this manuscript may assist clinical teams to promptly diagnose and holistically manage young patients with lipodystrophy syndromes and help optimize clinical outcomes as they transition to adult care.

Indexed as

LipodystrophyAdolescentChildChild, PreschoolFemaleHumansMaleacquired generalized lipodystrophyacquired partial lipodystrophyadolescentcomorbiditiescongenital generalized lipodystrophyfamilial partial lipodystrophymetreleptinpediatric

Identifiers

PMID40842493
PMCPMC12366100

What OpenQuestion holds

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Registered trials

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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.