Evidence map›Paper›PMID 33164942›Full record

ArticleJournal of neuromuscular diseases2021

Diagnosing X-linked Myotubular Myopathy - A German 20-year Follow Up Experience.

Andrea Gangfuss, Dirk Schmitt, Andreas Roos, Frederik Braun, Melanie Annoussamy, Laurent Servais, Ulrike Schara-Schmidt

Open access · hybridAbstract readCase ReportsComparative Study
In one paragraph

Article in Journal of neuromuscular diseases, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

10 citing papers in PubMed, 23 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. [Clinical and genetic features of 5 neonates with centronuclear myopathy caused byZhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics
    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

7 authors at 3 institutions in 4 countries.

Andrea GangfussDepartment of Neuropediatrics and Neuromuscular Centre for Children and Adolescents, University Children's Hospital Essen, University Duisburg-Essen, Essen, Germany.
Dirk SchmittAudentes Therapeutics, San Francisco, CA, USA.
Andreas RoosDepartment of Neuropediatrics and Neuromuscular Centre for Children and Adolescents, University Children's Hospital Essen, University Duisburg-Essen, Essen, Germany.
Frederik BraunDepartment of Neuropediatrics and Neuromuscular Centre for Children and Adolescents, University Children's Hospital Essen, University Duisburg-Essen, Essen, Germany.
Melanie AnnoussamyI-Motion, Institute of Myology, Paris, France.
Laurent ServaisUniversity of Liège, Neuromuscular Disease Reference Center, Department of Pediatrics, Liege, Belgium.
Ulrike Schara-SchmidtDepartment of Neuropediatrics and Neuromuscular Centre for Children and Adolescents, University Children's Hospital Essen, University Duisburg-Essen, Essen, Germany.
University of Duisburg-Essen · DESysnav (France) · FRUniversity of Liège · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

X-linked myotubular myopathy (XLMTM) is a life-threatening rare neuromuscular disease, which is caused by pathogenic variants in the MTM1 gene. It has a large phenotypic heterogeneity, ranging from patients, who are able to walk independently to immobile patients who are only able to bring hand to mouth and depend on a respirator 24 hours a day every day. This suggests that ventilator requirements may not illustrate the full clinical picture of patients with XLMTM. At present, there is no curative therapy available, despite first promising results from ongoing gene therapy studies.In this study, we evaluated in detail the data from 13 German XLMTM patients, which was collected over a period of up to 20 years in our university hospital. We compared it to the international prospective longitudinal natural history study (NHS) data from 45 patients (containing 11 German patients). To highlight the broad phenotypic spectrum of the disease, we additionally focused on the clinical presentation of three cases at a glance.Comparing our data with the above mentioned natural history study, it appears the patients of the present German cohort seem to be more often severely affected, with higher frequency of non-ambulatory patients and patients on ventilation (and for longer time) and a higher proportion of patients needing a percutaneous endoscopic gastrostomy. Another key finding is a potential gap in time between first clinical presentation and final diagnosis, showing a need for patients to be treated in a specialized center for neuromuscular diseases.

Indexed as

AdolescentAdultChildChild, PreschoolFollow-Up StudiesGermanyHumansLongitudinal StudiesMaleMyopathies, Structural, CongenitalOutcome Assessment, Health CareYoung AdultAAV-8breathing supportcentronuclear myopathycongenital myopathygene therapymotor milestonesmyotubularinX-linked myotubular myopathy

Identifiers

PMID33164942
PMCPMC7902950
OpenAlexW3097771892

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.