Evidence map›Paper›PMID 36708490›Full record

ArticleApplied biochemistry and biotechnology2023

Genetic Analysis of a Case of Sotos Syndrome with Suspected Germinal Mosaicism in Mother.

Xiao Hai, Guo Liangjie, Zhang Qian, Li Tao, Wang Hongdan, Kang Bing, Yang Ke, Guo Qiannan, Wu Dong, Liao Shixiu

Abstract readCase Reports
PubMed Publisher
In one paragraph

Article in Applied biochemistry and biotechnology, 2023. 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
0.3field-weighted citation impact, top 32% 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

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

10 authors at 2 institutions in 1 country.

Xiao HaiMedical Genetics Institute of Henan Province, Henan Provincial Peoples Hospital, Zhengzhou, 450003, Henan, China.
Guo LiangjieMedical Genetics Institute of Henan Province, Henan Provincial Peoples Hospital, Zhengzhou, 450003, Henan, China.
Zhang QianMedical Genetics Institute of Henan Province, Henan Provincial Peoples Hospital, Zhengzhou, 450003, Henan, China.
Li TaoDepartment of Medical Laboratory of Central China Fuwai Hospital, Zhengzhou, 450003, Henan, China.
Wang HongdanMedical Genetics Institute of Henan Province, Henan Provincial Peoples Hospital, Zhengzhou, 450003, Henan, China.
Kang BingMedical Genetics Institute of Henan Province, Henan Provincial Peoples Hospital, Zhengzhou, 450003, Henan, China.
Yang KeMedical Genetics Institute of Henan Province, Henan Provincial Peoples Hospital, Zhengzhou, 450003, Henan, China.
Guo QiannanMedical Genetics Institute of Henan Province, Henan Provincial Peoples Hospital, Zhengzhou, 450003, Henan, China.
Wu DongMedical Genetics Institute of Henan Province, Henan Provincial Peoples Hospital, Zhengzhou, 450003, Henan, China.
Liao ShixiuMedical Genetics Institute of Henan Province, Henan Provincial Peoples Hospital, Zhengzhou, 450003, Henan, China. shixiul2022@163.com.
Henan Provincial People's Hospital · CNZhengzhou Central Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study is to identify the pathogenic mutation of a child with Sots syndrome and provide prenatal diagnosis for his pregnant mother. Chromosome microarray technology was used to detect whether there were minor deletions/duplication in patients' chromosomes. The gene mutation of patients was screened by next-generation sequencing technology, and it was verified by Sanger sequencing. Prenatal diagnosis of the fetus was conducted according to the selected pathogenic sites, and genetic counseling was conducted for her parents. Chromosome microarray results showed that there was no minor deletion in a chromosome 5q35 region, and the second-generation sequencing results showed that there was a c.4138delG heterozygous mutation in the patient's NSD1 gene, and the pathogenic of this mutation was not reported in related databases. Sanger sequencing found that there was a c.4138delG heterozygous mutation in the NSD1 gene of the patient and her parents' genotype at this locus was wild type. The prenatal gene test results indicated that there was heterozygous mutation of NSD1 gene c.4138delG in the fetus, so it was suggested to terminate the pregnancy. Gentling results indicated that the fetus and the patient inherited the same maternal chromosome 5. The heterozygous mutation of NSD1 gene c.4138delG is the pathogenic mutation of this Sots syndrome patient, and the mother may be germinal mosaicism.

Indexed as

Sotos SyndromeChildFemaleHistone-Lysine N-MethyltransferaseHistone MethyltransferasesHumansMosaicismMothersPhenotypeHistone-Lysine N-MethyltransferaseHistone MethyltransferasesGerminal mosaicismNext-generation sequencingNovel mutationPrenatal diagnosisSotos syndrome

Identifiers

PMID36708490
OpenAlexW4318336416

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.