Evidence map›Paper›PMID 40893938›Full record

ArticleFrontiers in genetics2025

Case Report: Hereditary neuropathy with liability to pressure palsy (HNPP): the role of genetic investigation in diagnostic assessment.

Salvatore Savasta, Fabiola Serra, Lucrezia Galimberti, Francesco Fabrizio Comisi, Marcello Cossu, Alessandro Vannelli, Maddalena Masala, Sara Tanca, Stefania Murru

Abstract readCase Reports
In one paragraph

Article in Frontiers in genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–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

2 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Genes · 2025
    Pooled it
  2. 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.

Salvatore SavastaPediatric and Rare Diseases Clinic, Microcitemico Hospital "A. Cao", Department of Medical Sciences and Public Health, University of Cagliari, Cagliari, Italy.
Fabiola SerraPediatric and Rare Diseases Clinic, Microcitemico Hospital "A. Cao", University of Cagliari, Cagliari, Italy.
Lucrezia GalimbertiPediatric and Rare Diseases Clinic, Microcitemico Hospital "A. Cao", University of Cagliari, Cagliari, Italy.
Francesco Fabrizio ComisiPediatric and Rare Diseases Clinic, Microcitemico Hospital "A. Cao", University of Cagliari, Cagliari, Italy.
Marcello CossuPediatric and Rare Diseases Clinic, Microcitemico Hospital "A. Cao", University of Cagliari, Cagliari, Italy.
Alessandro VannelliBinaghi Hospital, ASL8, Cagliari, Italy.
Maddalena MasalaGenetic and Genomic Laboratory, Pediatric Children Hospital "A. Cao", ASL 8, Cagliari, Italy.
Sara TancaGenetic and Genomic Laboratory, Pediatric Children Hospital "A. Cao", ASL 8, Cagliari, Italy.
Stefania MurruGenetic and Genomic Laboratory, Pediatric Children Hospital "A. Cao", ASL 8, Cagliari, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hereditary neuropathy with liability to pressure palsies (HNPP) is a genetic disorder characterized by recurrent focal neuropathies typically occurring at sites of nerve entrapment or compression. It is classically described as a painless condition; however, pain is frequently reported. Due to its rarity and variable clinical presentation, HNPP is often underdiagnosed or initially misdiagnosed. We report the case of a 14-year-old girl who presented with sudden-onset arm weakness and pain following physical activity. The clinical presentation initially raised suspicion for a hereditary demyelinating neuropathy. Although there was no known family history, the patient's age and the persistence of symptoms supported the hypothesis of a genetic etiology. Neurophysiological studies were consistent with HNPP, which was subsequently confirmed by genetic testing. The primary aim of this report is to emphasize the importance of recognizing the early manifestations of HNPP-including pain, a symptom often underestimated or overlooked-in order to enable prompt diagnosis, reduce unnecessary diagnostic delays, and ensure timely initiation of appropriate genetic counseling. This case supports the notion that pain may represent an early feature of HNPP and should not lead clinicians away from considering this diagnosis.

Indexed as

childdemyelinatingdiagnosisgeneticshereditaryHNPPneuropathypalsy

Identifiers

PMID40893938
PMCPMC12391093

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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.