Evidence map›Paper›PMID 30567110›Full record

ArticleBMJ case reports2018

Dyskeratosis congenita: presentation of cutaneous triad in a sporadic case.

Reena Kumari Sharma, Mudita Gupta, Samriti Sood, Archit Gupta

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

Article in BMJ case reports, 2018. 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
0.3field-weighted citation impact, top 39% 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, 8 citations in OpenAlex.

  1. Article
  2. Case report: A novel mutation inFrontiers in oncology · 2023
    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.

Reena Kumari SharmaDepartment of Dermatology, Indira Gandhi Medical College, Shimla, Himachal Pradesh, India.
Mudita GuptaDepartment of Dermatology, Indira Gandhi Medical College, Shimla, Himachal Pradesh, India.
Samriti SoodDepartment of Dermatology, Indira Gandhi Medical College, Shimla, Himachal Pradesh, India.
Archit GuptaDepartment of Surgery, Indira Gandhi Medical College, Shimla, Himachal Pradesh, India.ORCID http://orcid.org/0000-0002-9476-2000
Indira Gandhi Medical College · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dyskeratosis congenita (DKC) also known as Zinsser-Cole-Engman syndrome is a progressive genetic disease with a classical presentation characterised by a triad of reticulate pigmentation of skin, nail dystrophy and leukoplakia. It may be a multisystem disease with the involvement of haematological, gastrointestinal, genitourinary, neurological, ophthalmic, pulmonary and skeletal system. We report a sporadic case of DKC presenting with poikiloderma, nail dystrophy and oral leukoplakia.

Indexed as

AdultAftercareDiagnosis, DifferentialDyskeratosis CongenitaGastrointestinal TractHumansLeukoplakia, OralMaleNail DiseasesNails, MalformedPigmentation DisordersSkindermatologyskin cancer

Identifiers

PMID30567110
PMCPMC6301648
OpenAlexW2904780385

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.