Evidence map›Paper›PMID 31388111›Full record

ArticleJournal of human genetics2019

Identification of novel variants in a large cohort of children with Tay-Sachs disease: An initiative of a multicentric task force on lysosomal storage disorders by Government of India.

Mehul Mistri, Sanjeev Mehta, Dhaval Solanki, Mahesh Kamate, Neerja Gupta, Madhulika Kabra, Ratna Puri, Katta Girisha, Sankar Hariharan, Sheela Nampoothiri and 2 more

Abstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Journal of human genetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 32% 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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Perspectives on the future of dysmorphology.American journal of medical genetics. Part A · 2023
    Article
  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

12 authors at 6 institutions in 2 countries.

Mehul MistriFRIGE's Institute of Human Genetics, Ahmedabad, Gujarat, India.
Sanjeev MehtaUsha Deep Hospital, Naranpura, Ahmedabad, Gujarat, India.
Dhaval SolankiMantra Child Neurology & Epilepsy Clinic, Bhavnagar, Gujarat, India.
Mahesh KamateKLES Prabhakar Kore Hospital, Belgaum, Karnataka, India.
Neerja GuptaAll India Institute of Medical Sciences (AIIMS), New Delhi, India.
Madhulika KabraAll India Institute of Medical Sciences (AIIMS), New Delhi, India.
Ratna PuriSir Ganga Ram Hospital, New Delhi, India.
Katta GirishaKasturba Medical College, Manipal, Karnataka, India.
Sankar HariharanSAT Hospital, Thiruvanathapuram, Trivandrum, India.
Sheela NampoothiriAmrita Institute of Medical Science & Research Centre, Kochi, Kerala, India.
Frenny ShethFRIGE's Institute of Human Genetics, Ahmedabad, Gujarat, India.ORCID http://orcid.org/0000-0001-8315-9436
Jayesh ShethFRIGE's Institute of Human Genetics, Ahmedabad, Gujarat, India. jshethad1@gmail.com.
All India Institute of Medical Sciences · INAmrita Institute of Medical Sciences and Research Centre · INInstitute of Human Genetics · PLKasturba Medical College, Manipal · INKLE Society Hospital · INSir Ganga Ram Hospital · IN

Funding

Indian Council of Medical Research (ICMR) GIA/31(ii)/2014-DHR
6 · The paper itself

Abstract

Tay-Sachs disease (TSD) (OMIM) is a neurodegenerative lysosomal storage disorder caused due to mutations in the HEXA gene. To date, nearly 190 mutations have been reported in HEXA gene. Here, we have characterized 34 enzymatically confirmed TSD families to investigate the presence of novel as well as known variants in HEXA gene. Overall study detected 25 variants belonging to 31 affected TSD patients and 3 carrier couples confirmed by enzyme study. Of these 17 patients harbors 15 novel variants, including seven missense variants [p.V206L, p.Y213H, p.R252C, p.F257S, p.C328G, p.G454R, and p.P475R], four nonsense variant [p.S9X, p.E91X, p.W420X, and p.W482X], two splice site variants [c.347-1G>A and c.460-1G>A], and two small deletion [c.1349delC (p.A450VfsX3) and c.52delG (p.G18Dfs*82)]. While remaining 17 patients harbors 10 previously reported variants that includes six missense variants [p.M1T, p.R170Q, p.D322Y, p.D322N, p.E462V, and p.R499C], one nonsense variant [p.Q106X], two splice site variants [c.1073+1G>A and c.459+4A>G] and one 4 bp insertion [c.1278insTATC (p.Y427IfsX5)]. In conclusion, Indian infantile TSD patients provide newer insight into the molecular heterogeneity of the TSD. Combining present study and our earlier studies, we have observed that 67% genotypes found in Indian TSD patients are novel, which are associated with severe infantile phenotypes, while rest 33% genotypes found in our cohort were previously reported in various populations. In addition, higher frequency of the p.E462V and c.1278insTATC mutations in the present study further support and suggest the prevalence of p.E462V mutation in the Indian population.

Indexed as

Allelesbeta-Hexosaminidase alpha ChainChild, PreschoolCodon, NonsenseDemographyFemaleGenetic Association StudiesHumansIndiaInfantMaleMutation, MissenseSequence DeletionTay-Sachs Diseasebeta-Hexosaminidase alpha ChainCodon, NonsenseHEXA protein, human

Identifiers

PMID31388111
OpenAlexW2965481364

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.