Evidence map›Paper›PMID 28399120›Full record

ArticlePediatric research2017

Sotos syndrome associated with Hirschsprung's disease: a new case and exome-sequencing analysis.

Cherry Ann Sio, Kyuwhan Jung, Jeong-Hyun Kim, Hyun Sub Cheong, Eun Shin, Hyejin Jang, Miok Yoon, Huijeong Jang, Hyoung Doo Shin

Open access · bronzeAbstract readCase Reports
PubMed Publisher
In one paragraph

Article in Pediatric research, 2017. 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
0.2field-weighted citation impact, top 42% 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

9 authors at 4 institutions in 1 country.

Cherry Ann SioDepartment of Surgery, Seoul National University Bundang Hospital, Seongnam, Gyeonggi, Republic of Korea.
Kyuwhan JungDepartment of Surgery, Jeju National University Hospital, Jeju, Republic of Korea.
Jeong-Hyun KimResearch Institute for Basic Science, Sogang University, Seoul, Republic of Korea.
Hyun Sub CheongDepartment of Genetic Epidemiology, SNP Genetics, Seoul, Republic of Korea.
Eun ShinDepartment of Pathology, Seoul National University Bundang Hospital, Seongnam, Gyeonggi, Republic of Korea.
Hyejin JangDepartment of Surgery, Seoul National University Bundang Hospital, Seongnam, Gyeonggi, Republic of Korea.
Miok YoonDepartment of Surgery, Seoul National University Bundang Hospital, Seongnam, Gyeonggi, Republic of Korea.
Huijeong JangDepartment of Surgery, Seoul National University Bundang Hospital, Seongnam, Gyeonggi, Republic of Korea.
Hyoung Doo ShinResearch Institute for Basic Science, Sogang University, Seoul, Republic of Korea.
Seoul National University Bundang Hospital · KRInstitute for Basic Science · KRJeju National University Hospital · KRSNP Genetics (South Korea) · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BackgroundSotos syndrome (SoS) is an overgrowth disorder with various congenital anomalies and is usually accompanied by other clinical problems. However, anorectal malformations have not been documented as part of the SoS entity. Our objective is to report on a case of SoS associated with Hirschsprung's disease (HSCR) and subsequent genetic analysis.MethodsA 2-year-old boy with SoS experienced constipation since infancy and ultimately showed an aganglionic segment in the histopathologic examination, which was followed by exome-sequencing analysis.ResultsIn the genetic test for SoS diagnosis, two novel mutations of NDS1, c.2465C>A (p.Ser822Tyr) and c.4347T>A (p.Cys1449*), were observed and verified by resequencing in the patient and his parents. In further whole-exome-sequencing analysis using the patient's blood DNA, which was followed by a comparison analysis with the results of our previously reported genome-wide association study (GWAS) of HSCR, three genes (ZNF827, FGD2, and KCNJ12) with significance for HSCR from our previous GWAS were overlapped among the genes showing variants in the exome sequencing.ConclusionThis is the first reported patient with SoS and HSCR. Further studies are required to determine whether there is a genetic relationship between SoS and HSCR.

Indexed as

Child, PreschoolDNAExomeFemaleGenetic TestingGenome-Wide Association StudyHirschsprung DiseaseHumansMaleMutationPedigreeSequence Analysis, DNASotos SyndromeDNA

Identifiers

PMID28399120
OpenAlexW2606115133

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.