Evidence map›Paper›PMID 37009284›Full record

ArticleFrontiers in pediatrics2023

Case report: Prader-Willi syndrome and inflammatory arthritis-An important consideration.

Luca Marelli, Tomáš Dallos, Elisabetta Miserocchi, Paolo Nucci, Beatrice Tombolini, Orazio De Lucia, Maurizio Gattinara, Roberto Caporali, Achille Marino

Open access · goldAbstract readCase Reports
In one paragraph

Article in Frontiers in pediatrics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 31% of its field
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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

9 authors at 6 institutions in 2 countries.

Luca MarelliEye Clinic San Giuseppe Hospital, IRCCS Multimedica Scientific Institute, Milan, Italy.
Tomáš DallosSecond Department of Pediatrics, Comenius University Medical School, Bratislava, Slovakia.
Elisabetta MiserocchiSchool of Medicine, Vita-Salute San Raffaele University, Milan, Italy.
Paolo NucciDepartment of Biomedical, Surgical and Dental Sciences, University of Milan, Milan, Italy.
Beatrice TomboliniSchool of Medicine, Vita-Salute San Raffaele University, Milan, Italy.
Orazio De LuciaDivision of Clinical Rheumatology, ASST G.Pini-CTO, Milano, Italy.
Maurizio GattinaraUnit of Pediatric Rheumatology, ASST G.Pini-CTO, Milan, Italy.
Roberto CaporaliDivision of Clinical Rheumatology, ASST G.Pini-CTO, Milano, Italy.
Achille MarinoUnit of Pediatric Rheumatology, ASST G.Pini-CTO, Milan, Italy.
Istituto Ortopedico Gaetano Pini · ITComenius University Bratislava · SKIstituti di Ricovero e Cura a Carattere Scientifico · ITMultiMedica · ITUniversity of Milan · ITVita-Salute San Raffaele University · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Prader-Willi syndrome (PWS) is a multisystemic genetically determined disorder. Musculoskeletal manifestations are common in most patients. We report the cases of two children with PWS who developed inflammatory arthritis, complicated with chronic anterior bilateral uveitis in one case. To our knowledge, no previous reports of such an association exist. Case presentation: Case 1 was of a 3-year-old girl diagnosed with PWS who developed arthritis of the right knee with morning stiffness, joint swelling, and limited range of motion. Other causes of arthritis were ruled out. Increased inflammatory markers, antinuclear antibody (ANA) positivity, and hypertrophic synovitis on ultrasound confirmed the diagnosis of inflammatory arthritis compatible with juvenile idiopathic arthritis (JIA). Despite the treatment with methotrexate, arthritis progressed, and etanercept was added. The patient reached and maintained articular remission while on combined MTX and etanercept treatment during 9 years of follow-up. Case 2 was of a 6-year-old boy diagnosed with PWS who developed arthritis of the right knee. Laboratory investigations showed mildly increased acute phase reactants, microcytic anemia, and ANA positivity at high titer (titer 1:1,280). Infectious and other causes of arthritis were excluded. Ultrasound confirmed the presence of joint effusion and synovial thickening, and synovial fluid analysis was consistent with inflammatory arthrosynovitis (white blood cell count of 14,200/µl) compatible with JIA. Shortly after the diagnosis, the ophthalmologic evaluation revealed the presence of bilateral anterior uveitis. Despite MTX and topical corticosteroid, ocular inflammation persisted and adalimumab was added. At the last follow-up, 9 months later, the child experienced inactivity of arthritis and uveitis with normal growth. Conclusions: We aim to raise awareness of this possible association among pediatricians since arthritis might be underestimated due to high pain tolerance, behavioral disturbances, and other musculoskeletal abnormalities in PWS patients.

Indexed as

arthritisgenetic disordershuman growth hormonejuvenile Idiopathic arthritisobesityPrader-Willi syndromeuveitis

Identifiers

PMID37009284
PMCPMC10063871
OpenAlexW4327734203

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.