Evidence map›Paper›PMID 35495804›Full record

ArticleJournal of family medicine and primary care2022

Smith-magenis syndrome: A rare case report.

Rupam Sinha, Harshvardhan Jha, Debarati Deb, Mainak Datta

Abstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Journal of family medicine and primary care, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. A Case of Smith-Magenis Syndrome Undergoing Palatoplasty.Journal of plastic and reconstructive surgery · 2026
    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

4 authors.

Rupam SinhaDepartment of Oral Medicine and Radiology, Haldia Institute of Dental Sciences and Research, Banbishnupur, Balughata Rd, West Bengal, India.
Harshvardhan JhaDepartment of Oral Medicine and Radiology, Haldia Institute of Dental Sciences and Research, Banbishnupur, Balughata Rd, West Bengal, India.
Debarati DebDepartment of Oral Medicine and Radiology, Haldia Institute of Dental Sciences and Research, Banbishnupur, Balughata Rd, West Bengal, India.
Mainak DattaDepartment of Oral Medicine and Radiology, Haldia Institute of Dental Sciences and Research, Banbishnupur, Balughata Rd, West Bengal, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Smith-Magenis syndrome is a rare genetic disorder involving multiple body systems, along with mental retardation and sleep disturbances. It is attributed to micro deletion at 17p11.2 chromosome region encoding for RAI1 gene. This article presents a case report of a 7-year-old patient having this rare syndrome along with his genetic analysis.

Indexed as

17p11.2 chromosomegeneticmental retardationRAI1 genesleep disturbances

Identifiers

PMID35495804
PMCPMC9051676

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.