Evidence map›Paper›PMID 25859498›Full record

ArticleJournal of clinical and diagnostic research : JCDR2015

Incontinentia pigmenti: a rare genodermatosis in a male child.

Dinesh Kumar Narayana Swamy, Arulkumaran Arunagirinathan, Revathi Krishnakumar, Sivaraman Sangili

Open access · goldAbstract readCase Reports
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 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 22% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Article
  3. 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.

Dinesh Kumar Narayana SwamyAssistant Professor, Department of Paediatrics, Sri Manakula Vinayagar Medical College and Hospital , Puducherry, India .
Arulkumaran ArunagirinathanAssociate Professor, Department of Paediatrics, Sri Manakula Vinayagar Medical College and Hospital , Puducherry, India .
Revathi KrishnakumarPost Graduate, Department of Paediatrics, Sri Manakula Vinayagar Medical College and Hospital , Puducherry, India .
Sivaraman SangiliPost Graduate, Department of Paediatrics, Sri Manakula Vinayagar Medical College and Hospital , Puducherry, India .
Sri Manakula Vinayagar Medical College and Hospital · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Incontinentia pigmenti is rare X-linked dominant disorder. There is no consistent expression of Incontinetia pigmenti in female child, but in male child, they always lead to death in utero. Vesicular, verrucous, hyperpigmented, and atrophic stages are the four stages of Incontinetia Pigmenti and it is uncommon for all stages to be seen in a same case. It is a rare genodermatosis, with only very few cases of male child with Incontinentia pigmenti have been reported. Thus, we report this case due to its extreme rarity and the child showed all the first 3 stages on followup.

Indexed as

EosinophiliaGenes X-LinkedMelaninsPigmentation

Identifiers

PMID25859498
PMCPMC4378780
OpenAlexW2114417421

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.