Evidence map›Paper›PMID 33433757›Full record

ArticleNeurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology2021

Lynch syndrome-associated repeated stroke with MLH1 frame-shift mutation.

Mengqi Zhang, Haojun Yang, Zhuohui Chen, Yishu Fan, Xinhang Hu, Weiping Liu

Erratum issuedAbstract readCase Reports
PubMed Publisher
In one paragraph

Article in Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 56% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Mengqi ZhangDepartment of Neurology, Xiangya Hospital of Central South University, Changsha, 410008, Hunan, China.
Haojun YangDepartment of Neurology, Xiangya Hospital of Central South University, Changsha, 410008, Hunan, China.
Zhuohui ChenDepartment of Neurology, Xiangya Hospital of Central South University, Changsha, 410008, Hunan, China.
Yishu FanDepartment of Neurology, Xiangya Hospital of Central South University, Changsha, 410008, Hunan, China.
Xinhang HuDepartment of Neurology, Xiangya Hospital of Central South University, Changsha, 410008, Hunan, China.
Weiping LiuDepartment of Neurology, Xiangya Hospital of Central South University, Changsha, 410008, Hunan, China. Liuwp@csu.edu.cn.ORCID http://orcid.org/0000-0001-6323-0557
Central South University · CN

Funding

Hunan Provincial Natural Science Foundation 2016JJ3174Hunan Provincial Natural Science Foundation General Project 2020JJ4134Hunan Provincial Natural Science Foundation General Project 2020JJ4893National Natural Science Foundation 81501025
6 · The paper itself

Abstract

Lynch syndrome (LS) is an autosomal dominant inherited disease caused by germline mutations in DNA mismatch repair (MMR) genes, including MLH1, MSH2, MSH6, and PMS2, which predisposes patients to various malignant neoplasms. Previous studies showed that MLH1, MSH2, MSH6, and PMS2 mutation in LS were associated with an elevated risk of colorectal, gastric, endometria, ovarian, and other cancers among family members. Patients of these kinds of cancers had high incidence of synchronous and metasynchronus. We describe the case of a 34-year-old female patient with 50 days of sudden dizziness and left limb weakness, whose head CT scan showed large infarction in the right frontal temporal parietal lobe and basal ganglia area. Imaging examinations and pathological biopsy indicated high-grade serous carcinoma (HGSC) IIIA1 of the right ovary. In addition, a novel frame-shift mutation in the MLH1 gene (c.1621dupG, p.A541Gfs*16) was found in the genetic panel sequence. It may render declining of MLH1 protein and also associate with the patient's progressive clinical manifestations of multiple systems. Therefore, the timely use of prenatal diagnosis to prevent unnecessary new cases of this severe genetic disease is available.

Indexed as

Colorectal Neoplasms, Hereditary NonpolyposisMutL Protein Homolog 1StrokeAdultDNA Mismatch RepairFemaleGenetic Predisposition to DiseaseHumansMutationMLH1 protein, humanMutL Protein Homolog 1Lynch syndromeMLH1MutationOvary cancer

Identifiers

PMID33433757
OpenAlexW3119455640

What OpenQuestion holds

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Read underepoch 390

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.