Evidence map›Paper›PMID 31519716›Full record

ArticleBMJ case reports2019

Unusual case of Juvenile Tay-Sachs disease.

Huma A Cheema, Nadia Waheed, Anjum Saeed

Open access · greenAbstract readCase Reports
In one paragraph

Article in BMJ case reports, 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
0.4field-weighted citation impact, top 35% 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, 6 citations in OpenAlex.

  1. Article
  2. 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

3 authors at 2 institutions in 2 countries.

Huma A CheemaDepartment of Pediatric Medicine, Division of Pediatric Gastroenterology, Hepatology and Nutrition, Children's Hospital and Institute of Child Health, Lahore, Pakistan.
Nadia WaheedDepartment of Pediatric Medicine, Division of Pediatric Gastroenterology, Hepatology and Nutrition, Children's Hospital and Institute of Child Health, Lahore, Pakistan.
Anjum SaeedDepartment of Pediatric Medicine, Division of Pediatric Gastroenterology, Hepatology and Nutrition, Children's Hospital and Institute of Child Health, Lahore, Pakistan.
Punjab Institute of Cardiology · PKInstitute of Child Health · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tay-Sachs disease (TSD) is a type 1 gangliosidosis (GM2) and caused by hexosaminidase A deficiency resulting in abnormal sphingolipid metabolism and deposition of precursors in different organs. It is a progressive neurodegenerative disorder transmitted in an autosomal-recessive manner. There is an accumulation of GM2 in neurocytes and retinal ganglions which result in progressive loss of neurological function and formation of the cherry-red spot which is the hallmark of TSD. We report the first case of juvenile TSD from Pakistan in a child with death of an older sibling without the diagnosis.

Indexed as

beta-Hexosaminidase alpha ChainChild, PreschoolExome SequencingGait Disorders, NeurologicHumansMaleMutationPakistanPalliative CareTay-Sachs Diseasebeta-Hexosaminidase alpha ChainHEXA protein, humanGeneticsMetabolic DisordersPaediatrics

Identifiers

PMID31519716
PMCPMC6747916
OpenAlexW2973088695

What OpenQuestion holds

Textmetadata
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.