Evidence map›Paper›PMID 35082614›Full record

ArticleCase reports in dermatology

Follicular Dowling-Degos Disease with Hidradenitis Suppurativa: A Case Report and Review of the Literature.

Ya-Nin Nokdhes, Thanachat Rutnumnoi, Poramin Patthamalai, Charussri Leeyaphan

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

Article in Case reports in dermatology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 37% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. The Genetics of Hidradenitis Suppurativa.Clinical, cosmetic and investigational dermatology · 2026
    Review
  2. Article
  3. About a Rare Association Between Vulvar Dowling Degos Disease and HS.International journal of women's health · 2023
    Article
  4. Article
  5. 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.

Ya-Nin NokdhesDepartment of Dermatology, Siriraj Hospital, Faculty of Medicine, Mahidol University, Bangkok, Thailand.
Thanachat RutnumnoiDepartment of Dermatology, Siriraj Hospital, Faculty of Medicine, Mahidol University, Bangkok, Thailand.
Poramin PatthamalaiDepartment of Dermatology, Siriraj Hospital, Faculty of Medicine, Mahidol University, Bangkok, Thailand.
Charussri LeeyaphanDepartment of Dermatology, Siriraj Hospital, Faculty of Medicine, Mahidol University, Bangkok, Thailand.
Siriraj Hospital · TH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dowling-Degos disease (DDD) is an autosomal dominant disorder with variable phenotypic expression. Classically, DDD is characterized by progressive reticulate hyperpigmentation on flexures with perioral pitted scars and comedone-like hyperkeratotic papules. Follicular DDD is a rare variant which was introduced by Singh et al. [

Indexed as

AcneFollicular Dowling-Degos diseaseHidradenitis suppurativa

Identifiers

PMID35082614
PMCPMC8739630
OpenAlexW3216342846

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.