Evidence map›Paper›PMID 37721175›Full record

ArticleBrain : a journal of neurology2024

Clinical and genetic characterisation of a large Indian congenital myasthenic syndrome cohort.

Kiran Polavarapu, Balaraju Sunitha, Ana Töpf, Veeramani Preethish-Kumar, Rachel Thompson, Seena Vengalil, Saraswati Nashi, Mainak Bardhan, Sai Bhargava Sanka, Akshata Huddar and 16 more

Open access · greenAbstract read
In one paragraph

Article in Brain : a journal of neurology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

13 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Congenital myasthenic syndrome due to novelJournal of neuromuscular diseases · 2026
    Article
  7. Article
  8. A clinical and genotype-phenotype analysis of MACF1 variants.American journal of human genetics · 2025
    Article
  9. Domain specific phenotypic expansion associated with variants inmedRxiv : the preprint server for health sciences · 2025
    Article
  10. Review
  11. A Multifaceted Giant Protein Microtubule-Actin Cross-Linking Factor 1.International journal of molecular sciences · 2025
    Review
  12. Article
  13. Review
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

26 authors at 9 institutions in 6 countries.

Kiran PolavarapuDepartment of Neurology, National Institute of Mental Health and Neurosciences, Bangalore 560029, India.ORCID 0000-0002-8879-6001
Balaraju SunithaJohn Walton Muscular Dystrophy Research Centre, Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne NE1 3BZ, UK.
Ana TöpfJohn Walton Muscular Dystrophy Research Centre, Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne NE1 3BZ, UK.
Veeramani Preethish-KumarDepartment of Neurology, National Institute of Mental Health and Neurosciences, Bangalore 560029, India.
Rachel ThompsonChildren's Hospital of Eastern Ontario Research Institute, Ottawa, ON K1H 8L1, Canada.ORCID 0000-0002-6889-0121
Seena VengalilDepartment of Neurology, National Institute of Mental Health and Neurosciences, Bangalore 560029, India.
Saraswati NashiDepartment of Neurology, National Institute of Mental Health and Neurosciences, Bangalore 560029, India.
Mainak BardhanDepartment of Neurology, National Institute of Mental Health and Neurosciences, Bangalore 560029, India.
Sai Bhargava SankaDepartment of Neurology, National Institute of Mental Health and Neurosciences, Bangalore 560029, India.
Akshata HuddarDepartment of Neurology, National Institute of Mental Health and Neurosciences, Bangalore 560029, India.
Gopikrishnan UnnikrishnanDepartment of Neurology, National Institute of Mental Health and Neurosciences, Bangalore 560029, India.
Gautham ArunachalDepartment of Human Genetics, National Institute of Mental Health and Neurosciences, Bengaluru 560029, India.
Manu Santhappan GirijaDepartment of Neurology, National Institute of Mental Health and Neurosciences, Bangalore 560029, India.
Anna PorterJohn Walton Muscular Dystrophy Research Centre, Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne NE1 3BZ, UK.
Yoshiteru AzumaJohn Walton Muscular Dystrophy Research Centre, Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne NE1 3BZ, UK.
Paulo José LorenzoniNeuromuscular Disorders Division, Service of Neurology, Department of Internal Medicine, Hospital de Clínicas, Universidade Federal do Paraná, Rua General Carneiro, Curitiba - PR 80060-900, Brazil.
Dipti BaskarDepartment of Neurology, National Institute of Mental Health and Neurosciences, Bangalore 560029, India.
Ram Murthy AnjanappaDepartment of Neurology, National Institute of Mental Health and Neurosciences, Bangalore 560029, India.
Madassu KeertipriyaDepartment of Neurology, National Institute of Mental Health and Neurosciences, Bangalore 560029, India.
Hansashree PadmanabhDepartment of Neurology, National Institute of Mental Health and Neurosciences, Bangalore 560029, India.
Ganaraja Valakunja HarikrishnaDepartment of Neurology, National Institute of Mental Health and Neurosciences, Bangalore 560029, India.
Steve LaurieCentro Nacional de Análisis Genómico (CNAG-CRG), Center for Genomic Regulation, Barcelona Institute of Science and Technology (BIST), Barcelona, Catalonia 08028, Spain.
Leslie MatalongaCentro Nacional de Análisis Genómico (CNAG-CRG), Center for Genomic Regulation, Barcelona Institute of Science and Technology (BIST), Barcelona, Catalonia 08028, Spain.
Rita HorvathDepartment of Clinical Neurosciences, University of Cambridge School of Clinical Medicine, Cambridge CB2 0SP, UK.ORCID 0000-0002-9841-170X
Atchayaram NaliniDepartment of Neurology, National Institute of Mental Health and Neurosciences, Bangalore 560029, India.ORCID 0000-0001-9791-3639
Hanns LochmüllerChildren's Hospital of Eastern Ontario Research Institute, Ottawa, ON K1H 8L1, Canada.ORCID 0000-0003-2324-8001
National Institute of Mental Health and Neurosciences · INNewcastle University · GBCentro Nacional de Análisis Genómico · ESChildren's Hospital of Eastern Ontario · CAUniversity of Cambridge · GBAmrita Institute of Medical Sciences and Research Centre · INHospital de Clínicas Universidade Federal do Paraná · BRSt.John's Medical College Hospital · INUniversity of Ottawa · CA

Funding

Joint Center for Mendelian GenomicsUM1HG008900 · NHGRI · BROAD INSTITUTE, INC. · PI O'DONNELL-LURIA, ANNE, REHM, HEIDI L · 2016 to 2020
$16.5M
A powerful web-based discovery platform for rare disease geneticsR01HG009141 · NHGRI · BROAD INSTITUTE, INC. · PI QUINLAN, AARON R, REHM, HEIDI L · 2017 to 2020
$2.9M
NEI NIH HHSNHGRI NIH HHS R01 HG009141NHGRI NIH HHS UM1 HG008900
6 · The paper itself

Abstract

Congenital myasthenic syndromes (CMS) are a rare group of inherited disorders caused by gene defects associated with the neuromuscular junction and potentially treatable with commonly available medications such as acetylcholinesterase inhibitors and β2 adrenergic receptor agonists. In this study, we identified and genetically characterized the largest cohort of CMS patients from India to date. Genetic testing of clinically suspected patients evaluated in a South Indian hospital during the period 2014-19 was carried out by standard diagnostic gene panel testing or using a two-step method that included hotspot screening followed by whole-exome sequencing. In total, 156 genetically diagnosed patients (141 families) were characterized and the mutational spectrum and genotype-phenotype correlation described. Overall, 87 males and 69 females were evaluated, with the age of onset ranging from congenital to fourth decade (mean 6.6 ± 9.8 years). The mean age at diagnosis was 19 ± 12.8 (1-56 years), with a mean diagnostic delay of 12.5 ± 9.9 (0-49 years). Disease-causing variants in 17 CMS-associated genes were identified in 132 families (93.6%), while in nine families (6.4%), variants in genes not associated with CMS were found. Overall, postsynaptic defects were most common (62.4%), followed by glycosylation defects (21.3%), synaptic basal lamina genes (4.3%) and presynaptic defects (2.8%). Other genes found to cause neuromuscular junction defects (DES, TEFM) in our cohort accounted for 2.8%. Among the individual CMS genes, the most commonly affected gene was CHRNE (39.4%), followed by DOK7 (14.4%), DPAGT1 (9.8%), GFPT1 (7.6%), MUSK (6.1%), GMPPB (5.3%) and COLQ (4.5%). We identified 22 recurrent variants in this study, out of which eight were found to be geographically specific to the Indian subcontinent. Apart from the known common CHRNE variants p.E443Kfs*64 (11.4%) and DOK7 p.A378Sfs*30 (9.3%), we identified seven novel recurrent variants specific to this cohort, including DPAGT1 p.T380I and DES c.1023+5G>A, for which founder haplotypes are suspected. This study highlights the geographic differences in the frequencies of various causative CMS genes and underlines the increasing significance of glycosylation genes (DPAGT1, GFPT1 and GMPPB) as a cause of neuromuscular junction defects. Myopathy and muscular dystrophy genes such as GMPPB and DES, presenting as gradually progressive limb girdle CMS, expand the phenotypic spectrum. The novel genes MACF1 and TEFM identified in this cohort add to the expanding list of genes with new mechanisms causing neuromuscular junction defects.

Indexed as

Myasthenic Syndromes, CongenitalAcetylcholinesteraseAdolescentAdultChildDelayed DiagnosisFemaleGenetic TestingHumansMaleMutationNeuromuscular JunctionYoung AdultAcetylcholinesterasecongenital myasthenic syndromesgeneticsneuromuscular junctionNGSrecurrent mutations

Identifiers

PMID37721175
PMCPMC10766255
OpenAlexW4386818355

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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.