Evidence map›Paper›PMID 29977664›Full record

ArticlePeerJ2018

Distinctive facial features in idiopathic Moyamoya disease in Caucasians: a first systematic analysis.

Markus Kraemer, Quoc Bao Huynh, Dagmar Wieczorek, Brunilda Balliu, Barbara Mikat, Stefan Boehringer

Open access · goldAbstract read
In one paragraph

Article in PeerJ, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.8field-weighted citation impact, top 16% 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, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Quantification of Facial Traits.Frontiers in genetics · 2019
    Review
  4. 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 5 institutions in 3 countries.

Markus KraemerDepartment of Neurology, Alfried Krupp Hospital Essen, Essen, Germany.
Quoc Bao HuynhDepartment of Neurology, Alfried Krupp Hospital Essen, Essen, Germany.
Dagmar WieczorekInstitute of Human Genetics, University of Duesseldorf, Duesseldorf, Germany.
Brunilda BalliuInstitute of Genetics, Stanford University School of Medicine, Stanford, CA, United States of America.
Barbara MikatInstitute of Human Genetics, University of Essen, Essen, Germany.
Stefan BoehringerBiomedical Data Sciences, Leiden University Medical Center, Leiden, The Nederlands.
Essen University Hospital · DEAlfried Krupp Hospital · DEDüsseldorf University Hospital · DELeiden University Medical Center · NLStanford University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCraniofacial dysmorphic features are morphological changes of the face and skull which are associated with syndromic conditions. Moyamoya angiopathy is a rare cerebral vasculopathy that can be divided into Moyamoya syndrome, which is associated or secondary to other diseases, and into idiopathic Moyamoya disease. Facial dysmorphism has been described in rare genetic syndromes with associated Moyamoya syndrome. However, a direct relationship between idiopathic Moyamoya disease with dysmorphic facial changes is not known yet.

methodsLandmarks were manually placed on frontal photographs of the face of 45 patients with bilateral Moyamoya disease and 50 matched controls. After procrustes alignment of landmarks a multivariate, penalized logistic regression (elastic-net) was performed on geometric features derived from landmark data to classify patients against controls. Classifiers were visualized in importance plots that colorcode importance of geometric locations for the classification decision.

resultsThe classification accuracy for discriminating the total patient group from controls was 82.3% ( DISCUSSION: Results suggest that there is a resemblance in faces of Caucasian patients with idiopathic Moyamoya disease and that there is a difference to matched controls. Replication of findings is necessary as it is difficult to control all residual confounding in study designs such as ours. If our results would be replicated in a larger cohort, this would be helpful for pathophysiological interpretation and early detection of the disease.

Indexed as

FaceGenetic causesIdiopathicMoyamoya diseasePhotographsResemblance

Identifiers

PMID29977664
PMCPMC6029584
OpenAlexW2811434058

What OpenQuestion holds

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LicenceCC BY
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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.