Evidence map›Paper›PMID 25859481›Full record

ArticleJournal of clinical and diagnostic research : JCDR2015

Type 1 and type 3 Gaucher disease in two siblings in a family: 2 unusual case reports.

Dolanchampa Modak, Sasmit Roy, Uttam Nath, S K Guha

Open access · goldAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Journal of clinical and diagnostic research : JCDR, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. 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

4 authors at 1 institution in 1 country.

Dolanchampa ModakAssistant Professor, Department of Tropical Medicine, School of Tropical Medicine , Kolkata, India .
Sasmit RoyPost Graduate Trainee, Department of Tropical Medicine, School of Tropical Medicine , Kolkata, India .
Uttam NathAssistant Professor, Department of Hematology and Transfusion Medicine, Institute of Hematology & Transfusion Medicine , Kolkata, India .
S K GuhaProfessor, Department of Tropical Medicine, School of Tropical Medicine , Kolkata, India .
Hospital for Tropical Diseases · VN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gaucher disease (GD) is an autosomal recessive disorder, characterized by lack of acid β-glucosidase (glucocerebrosidase) enzyme resulting in accumulation of glucosylceramide in different organs. It is common in Ashkenazi Jews but rare in India. Around five hundred cases are identified and diagnosed in India. We are reporting two interesting cases of type 1 non-neuropathic and type 3 juvenile subacute neuropathic variant of adult Gaucher disease in two of three siblings in a family.

Indexed as

Gaucher diseaseGlucocerebrosidaseLysosomal storage disorderSibling

Identifiers

PMID25859481
PMCPMC4378763
OpenAlexW2139556124

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.