Evidence map›Paper›PMID 30838128›Full record

ArticleOxford medical case reports2019

Kindler syndrome: a rare case report from Greece.

Maria Gkaitatzi, Evangelia Kalloniati, Cristina Has, Dimitra Kiritsi, Theofanis Spiliopoulos, Sophia Georgiou

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

Article in Oxford medical case reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
0.2field-weighted citation impact, top 49% 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

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 4 citations in OpenAlex.

  1. Clinical practice guidelines: Oral health care for children and adults living with epidermolysis bullosa.Special care in dentistry : official publication of the American Association of Hospital Dentists, the Academy of Dentistry for the Handicapped, and the American Society for Geriatric Dentistry · 2020
    Pooled it
  2. Article
  3. Kindler syndrome: a rare case report from Syria.Annals of medicine and surgery (2012) · 2023
    Article
  4. A novel frameshift mutation in theExperimental and therapeutic medicine · 2020
    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

6 authors at 3 institutions in 2 countries.

Maria GkaitatziDepartment of Dermatology, University of Patras, Greece.
Evangelia KalloniatiDepartment of Dermatology, University of Patras, Greece.
Cristina HasDepartment of Dermatology, Medical Center-University of Freiburg, Faculty of Medicine, Freiburg, Germany.
Dimitra KiritsiDepartment of Dermatology, Medical Center-University of Freiburg, Faculty of Medicine, Freiburg, Germany.
Theofanis SpiliopoulosDepartment of Dermatology, University of Patras, Greece.
Sophia GeorgiouDepartment of Dermatology, University of Patras, Greece.
University of Patras · GRUniversity Medical Center Freiburg · DEUniversity of Freiburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Kindler syndrome is a rare autosomal recessive inherited disease characterized by infantile acral bullae, progressive poikiloderma, cutaneous atrophy, photosensitivity and various forms of mucosal involvement. In this paper, we report a case of a 49-year-old Greek Caucasian male aiming to emphasize the importance of genetic analysis as a gold standard of diagnosis.

Identifiers

PMID30838128
PMCPMC6396407
OpenAlexW2915642130

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.