Evidence map›Paper›PMID 26834495›Full record

ArticleThe application of clinical genetics2016

Case report of individual with cutaneous immunodeficiency and novel 1p36 duplication.

Alyn D Hatter, David C Soler, Christine Curtis, Kevin D Cooper, Thomas S McCormick

Open access · goldAbstract readCase Reports
In one paragraph

Article in The application of clinical genetics, 2016. 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
–field-weighted citation impact, top 100% 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, 3 citations in OpenAlex.

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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

5 authors at 3 institutions in 1 country.

Alyn D HatterUniversity Hospitals Case Medical Center, Cleveland, OH, USA.
David C SolerDepartment of Dermatology, Cleveland, OH, USA; The Murdough Family Center for Psoriasis, Case Western Reserve University, Cleveland, OH, USA.
Christine CurtisCleveland Department of Pathology and Center for Human Genetics Laboratory, Cleveland, OH, USA.
Kevin D CooperUniversity Hospitals Case Medical Center, Cleveland, OH, USA; Department of Dermatology, Cleveland, OH, USA; The Murdough Family Center for Psoriasis, Case Western Reserve University, Cleveland, OH, USA; VA Medical Center, Cleveland, OH, USA.
Thomas S McCormickDepartment of Dermatology, Cleveland, OH, USA; The Murdough Family Center for Psoriasis, Case Western Reserve University, Cleveland, OH, USA.
Case Western Reserve University · USCenter for Human Genetics · USUniversity Hospitals Case Medical Center · US

Funding

Vitamin D endocrine system and Protection Against Skin TumorlgenesisP30AR039750 · NIAMS · CASE WESTERN RESERVE UNIVERSITY · PI COOPER, KEVIN D · 1988 to 2015
$9.1M
NIAMS NIH HHS P30 AR039750
6 · The paper itself

Abstract

introductionCrusted or Norwegian scabies is an infectious skin dermatopathology usually associated with an underlying immunodeficiency condition. It is caused when the mite Sarcoptes scabiei infects the skin, and the immune system is unable to control its spread, leading to a massive hyperinfestation with a simultaneous inflammatory and hyperkeratotic reaction. This is the first report of a novel 1p36 duplication associated with a recurrent infection of crusted scabies. CASE REPORT: We describe a 34-year-old patient with a cutaneous immunodeficiency characterized by recurrent crusted scabies infestation, diffuse tinea, and recurrent staphylococcal cellulitis, who we suspected had an undiagnosed syndrome. The patient also suffered from mental retardation, renal failure, and premature senescence. A cytogenetic fluorescence in situ hybridization analysis revealed a 9.34 Mb duplication within the short (p) arm of chromosome 1, precisely from 1p36.11 to 1p36.21, with an adjacent 193 kb copy gain entirely within 1p36.11. In addition, chromosome 4 had a 906 kb gain in 4p16.1 and chromosome 9 had a 81 kb copy gain in 9p24.3. Over 100 genes localized within these duplicated regions. Gene expression array revealed 82 genes whose expression changed >1.5-fold compared to a healthy age-matched skin control, but among them only the lipolytic enzyme arylacetamide deacetylase-like 3 was found within the duplicated 1p36 region of chromosome 1. DISCUSSION: Although genetic duplications in the 1p36 region have been previously described, our report describes a novel duplicative variant within the 1p36 region. The patient did not have a past history of immunosuppression but was afflicted by a recurrent case of crusted scabies, raising the possibility that the recurrent infection was associated with the 1p36 genetic duplication.

conclusionTo our knowledge, the specific duplicated sequence between 1p36.11 and p36.21 found in our patient has never been previously reported. We reviewed and compared the clinical, genotyping, and gene microarray results of our patient in order to characterize this novel 1p36 duplication syndrome, which might have contributed to the recurrent scabies infection in this patient.

Indexed as

1p36 duplicationcrusted scabiescutaneous immunodeficiencyimmunodeficiency

Identifiers

PMID26834495
PMCPMC4716770
OpenAlexW2239732517

What OpenQuestion holds

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Registered trials

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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.