Evidence map›Paper›PMID 38379631›Full record

ArticleSAGE open medical case reports2024

Complex neuropsychiatric presentation of 17q12 duplication syndrome: A case report.

Soumitra Das, Lochana Samarasinghe, Sheryl Deva, Elaiza Marie Fernandez Co, Sujan Poudel, Tirth Dave, Sakshi Prasad, Ashish Sarangi

Open access · goldAbstract readCase Reports
In one paragraph

Article in SAGE open medical case reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 98% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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 6 institutions in 4 countries.

Soumitra DasDepartment of Psychiatry, Western Health, Footscray, VIC, Australia.
Lochana SamarasingheBase Hospital Nikaweratiya, Nikaweratiya, Srilanka.
Sheryl DevaKamineni Academy of Medical Sciences and Research Center, Hyderabad, Telangana, India.
Elaiza Marie Fernandez CoCebu Institute of Medicine, Cebu, Philippines.
Sujan PoudelLarkin Community Hospital, South Miami, FL, USA.
Tirth DaveBukovinian State Medical University, Chernivtsi, Ukraine.ORCID https://orcid.org/0000-0001-7935-7333
Sakshi PrasadVinnytsia National Pirogov Memorial Medical University, Vinnitsya, Ukraine.ORCID https://orcid.org/0000-0002-1014-9031
Ashish SarangiUniversity of Missouri, Columbia, MO, USA.
Bukovinian State Medical University · UAFootscray Hospital · AUKamineni Hospitals · INLarkin Community Hospital · USNational Pirogov Memorial Medical University, Vinnytsya · UAUniversity of Missouri · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The chromosomal band 17q12 is characterized by a high density of genes and is bordered by segmental duplications, the structural arrangement of which increases the susceptibility of the region to deletions and duplications. Duplication of 17q12 is a rare genetic condition associated with variable characteristics from clinically asymptomatic to intellectual disabilities, seizures, and behavioral problems. The variability in phenotype is primarily due to variable expressivity and incomplete penetrance. Diagnosis is mostly established by chromosomal microarray. Treatment involves a multidisciplinary approach. We present a case of a 43-year-old female who initially presented with hyperphagia and was eventually diagnosed with bulimia nervosa, anxiety, mood disorder, and personality disorder. Additional research is required to better understand the impact of 17q12 duplication syndrome on the development of bulimia nervosa since its pathogenesis has not been adequately described in the current literature.

Indexed as

17q12 duplicationbariatric surgerybulimia nervosacase reportdepressionobesity

Identifiers

PMID38379631
PMCPMC10878203
OpenAlexW4391927108

What OpenQuestion holds

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LicenceCC BY-NC
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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.