Evidence map›Paper›PMID 33960642›Full record

ArticleAmerican journal of medical genetics. Part A2021

Microdeletion of 9q22.3: A patient with minimal deletion size associated with a severe phenotype.

Adam D Ewing, Seth W Cheetham, James J McGill, Michael Sharkey, Rick Walker, Jennifer A West, Malcolm J West, Kim M Summers

Open access · hybridAbstract readCase Reports
In one paragraph

Article in American journal of medical genetics. Part A, 2021. 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
0.2field-weighted citation impact, top 48% 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

8 authors at 4 institutions in 1 country.

Adam D EwingMater Research Institute-University of Queensland, Translational Research Institute, Woolloongabba, Queensland, Australia.
Seth W CheethamMater Research Institute-University of Queensland, Translational Research Institute, Woolloongabba, Queensland, Australia.
James J McGillDepartment of Chemical Pathology, Royal Brisbane and Women's Hospital, Herston, Queensland, Australia.
Michael SharkeyPaddington Dermatology Specialist Clinic, Paddington, Queensland, Australia.
Rick WalkerQLD Youth Cancer Service, Queensland Children's Hospital, South Brisbane, Queensland, Australia.
Jennifer A WestNorthside Clinical School, Prince Charles Hospital, The University of Queensland, Chermside, Queensland, Australia.
Malcolm J WestNorthside Clinical School, Prince Charles Hospital, The University of Queensland, Chermside, Queensland, Australia.
Kim M SummersMater Research Institute-University of Queensland, Translational Research Institute, Woolloongabba, Queensland, Australia.ORCID 0000-0002-7084-4386
The University of Queensland · AUTranslational Research Institute · AUPaddington Cat Hospital · AURoyal Brisbane and Women's Hospital · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Basal cell nevus syndrome (also known as Gorlin Syndrome; MIM109400) is an autosomal dominant disorder characterized by recurrent pathological features such as basal cell carcinomas and odontogenic keratocysts as well as skeletal abnormalities. Most affected individuals have point mutations or small insertions or deletions within the PTCH1 gene on human chromosome 9, but there are some cases with more extensive deletion of the region, usually including the neighboring FANCC and/or ERCC6L2 genes. We report a 16-year-old patient with a deletion of approximately 400,000 bases which removes only PTCH1 and some non-coding RNA genes but leaves FANCC and ERCC6L2 intact. In spite of the small amount of DNA for which he is haploid, his phenotype is more extreme than many individuals with longer deletions in the region. This includes early presentation with a large number of basal cell nevi and other skin lesions, multiple jaw keratocysts, and macrosomia. We found that the deletion was in the paternal chromosome, in common with other macrosomia cases. Using public databases, we have examined possible interactions between sequences within and outside the deletion and speculate that a regulatory relationship exists with flanking genes, which is unbalanced by the deletion, resulting in abnormal activation or repression of the target genes and hence the severity of the phenotype.

Indexed as

AdolescentBasal Cell Nevus SyndromeChildChild, PreschoolChromosome DisordersChromosomes, Human, Pair 9DNA HelicasesFanconi Anemia Complementation Group C ProteinGenetic Predisposition to DiseaseHumansInfantInfant, NewbornMaleNeoplasm Recurrence, LocalOdontogenic CystsPatched-1 ReceptorDNA HelicasesERCC6L2 protein, humanFANCC protein, humanFanconi Anemia Complementation Group C ProteinPatched-1 Receptor9q22.3 deletionbasal cell nevus syndromeGorlin syndromePTCH1

Identifiers

PMID33960642
PMCPMC8251932
OpenAlexW3158903006

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.