Evidence map›Paper›PMID 38439002›Full record

ArticleBMC psychiatry2024

Cohen syndrome combined with psychiatric symptoms: a case report.

Xinming Li, Sufang Qi, Wenjie Li, Xin Liu, Zhicheng Xue, Tiangui Yu, Guanglei Xun

Open access · goldAbstract readCase Reports
In one paragraph

Article in BMC psychiatry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

2 citing papers in PubMed, 1 citations in OpenAlex.

  1. Article
  2. [Cohen syndrome in a child caused by compound heterozygous variants inZhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2025
    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

7 authors at 1 institution in 1 country.

Xinming LiShandong Mental Health Center, Shandong University, Mail Code: 250014, 49# Wenhua Eastern Road, Jinan, Shandong Province, P.R. China.
Sufang QiShandong Mental Health Center, Shandong University, Mail Code: 250014, 49# Wenhua Eastern Road, Jinan, Shandong Province, P.R. China.
Wenjie LiShandong Mental Health Center, Shandong University, Mail Code: 250014, 49# Wenhua Eastern Road, Jinan, Shandong Province, P.R. China.
Xin LiuShandong Mental Health Center, Shandong University, Mail Code: 250014, 49# Wenhua Eastern Road, Jinan, Shandong Province, P.R. China.
Zhicheng XueShandong Mental Health Center, Shandong University, Mail Code: 250014, 49# Wenhua Eastern Road, Jinan, Shandong Province, P.R. China.
Tiangui YuShandong Mental Health Center, Shandong University, Mail Code: 250014, 49# Wenhua Eastern Road, Jinan, Shandong Province, P.R. China. sdyutg@163.com.
Guanglei XunShandong Mental Health Center, Shandong University, Mail Code: 250014, 49# Wenhua Eastern Road, Jinan, Shandong Province, P.R. China. xungl@163.com.
Shandong Mental Health Center · CN

Funding

Research, development and demonstration application of key technologies for the prevention, diagnosis and treatment of major diseases in the field of public health 2021SFGC0504
6 · The paper itself

Abstract

backgroundCohen syndrome (CS) is a rare autosomal recessive inherited condition characterized by pathological changes affecting multiple systems. The extensive clinical variability associated with CS poses a significant diagnostic challenge. Additionally, there is limited documentation on the co-occurrence of CS with psychiatric symptoms. CASE REPORT: We report a case of a 30-year-old patient exhibiting characteristic physical features and psychiatric symptoms. Whole exome sequencing identified two heterozygous variants, a nonsense variation c.4336 C > T and a missense mutation c.4729G > A. Integrating clinical manifestations with genetic test results, we established the diagnosis of CS combined with psychiatric symptoms.

conclusionsThis case introduces a novel missense variant as a candidate in the expanding array of VPS13B pathogenic variants. Its clinical significance remains unknown, and further investigation may broaden the spectrum of pathogenic variants associated with the VPS13B gene. Early diagnosis of CS is crucial for the prognosis of young children and holds significant importance for their families.

Indexed as

Intellectual DisabilityMicrocephalyMuscle HypotoniaMyopiaObesityRetinal DegenerationAdultChildChild, PreschoolDevelopmental DisabilitiesDocumentationFingersHumansCohen syndromeGene mutationPsychiatric symptoms

Identifiers

PMID38439002
PMCPMC10913230
OpenAlexW4392382485

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.