Evidence map›Paper›PMID 34438578›Full record

ReviewChildren (Basel, Switzerland)2021

Differential Diagnosis of Acquired and Hereditary Neuropathies in Children and Adolescents-Consensus-Based Practice Guidelines.

Rudolf Korinthenberg, Regina Trollmann, Barbara Plecko, Georg M Stettner, Markus Blankenburg, Joachim Weis, Benedikt Schoser, Wolfgang Müller-Felber, Nina Lochbuehler, Gabriele Hahn and 1 more

Abstract readReview
In one paragraph

Review in Children (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

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

  1. Pooled it
  2. Article
  3. Article
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  5. Article
  6. Article
  7. Review
  8. 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

11 authors.

Rudolf KorinthenbergDivision of Neuropaediatrics and Muscular Disorders, Faculty of Medicine, University Medical Center (UMC), University of Freiburg, 79106 Freiburg, Germany.ORCID 0000-0002-4638-3460
Regina TrollmannDepartment of Pediatrics, Division of Neuropaediatrics, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), 91054 Erlangen, Germany.ORCID 0000-0001-6031-8537
Barbara PleckoDepartment of Pediatrics and Adolescent Medicine, Medical University Graz, 8036 Graz, Austria.ORCID 0000-0002-3203-1325
Georg M StettnerNeuromuscular Center Zurich, Department of Pediatric Neurology, University Children's Hospital Zurich, University of Zurich, 8032 Zurich, Switzerland.ORCID 0000-0002-0906-8816
Markus BlankenburgDepartment of Pediatric Neurology, Klinikum Stuttgart, Olgahospital, 70174 Stuttgart, Germany.ORCID 0000-0002-5595-0981
Joachim WeisInstitute of Neuropathology, RWTH Aachen University Hospital, 52074 Aachen, Germany.
Benedikt SchoserFriedrich-Baur-Institute, Department of Neurology, Ludwig-Maximilians-University of Munich, Ziemssenstr. 1a, 80336 Munich, Germany.ORCID 0000-0002-2757-8131
Wolfgang Müller-FelberDepartment of Neuropaediatrics, UMC, LMU Munich, 80337 Munich, Germany.
Nina LochbuehlerPediatric Radiology, Institute of Radiology, Olgahospital, Klinikum Stuttgart, 70174 Stuttgart, Germany.ORCID 0000-0001-9054-1377
Gabriele HahnDepartment of Radiological Diagnostics, UMC, University of Dresden, 01307 Dresden, Germany.
Sabine Rudnik-SchönebornDivision of Human Genetics, Medical University of Innsbruck, 6020 Innsbruck, Austria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Disorders of the peripheral nerves can be caused by a broad spectrum of acquired or hereditary aetiologies. The objective of these practice guidelines is to provide the reader with information about the differential diagnostic workup for a target-oriented diagnosis. Following an initiative of the German-speaking Society of Neuropaediatrics, delegates from 10 German societies dedicated to neuroscience worked in close co-operation to write this guideline. Applying the Delphi methodology, the authors carried out a formal consensus process to develop practice recommendations. These covered the important diagnostic steps both for acquired neuropathies (traumatic, infectious, inflammatory) and the spectrum of hereditary Charcot-Marie-Tooth (CMT) diseases. Some of our most important recommendations are that: (i) The indication for further diagnostics must be based on the patient's history and clinical findings; (ii) Potential toxic neuropathy also has to be considered; (iii) For focal and regional neuropathies of unknown aetiology, nerve sonography and MRI should be performed; and (iv) For demyelinated hereditary neuropathy, genetic diagnostics should first address PMP22 gene deletion: once that has been excluded, massive parallel sequencing including an analysis of relevant CMT-genes should be performed. This article contains a short version of the guidelines. The full-length text (in German) can be found at the Website of the "Arbeitsgemeinschaft der Wissenschftlichen Medizinischen Fachgesellschaften e.V. (AWMF), Germany.

Indexed as

adolescentsCharcot–Marie–Tooth diseasechildreninflammatory neuropathymetabolic neuropathyneuropathytraumatic neuropathy

Identifiers

PMID34438578
PMCPMC8392610

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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.