Evidence map›Paper›PMID 28349652›Full record

ArticleAmerican journal of medical genetics. Part A2017

Normal IQ is possible in Smith-Lemli-Opitz syndrome.

Yasemen Eroglu, Mina Nguyen-Driver, Robert D Steiner, Louise Merkens, Mark Merkens, Jean-Baptiste Roullet, Ellen Elias, Geeta Sarphare, Forbes D Porter, Chumei Li and 3 more

Open access · greenAbstract read
In one paragraph

Article in American journal of medical genetics. Part A, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

3 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Smith-Lemli-Opitz Syndrome: Bosnian and Herzegovinian Experience.Balkan journal of medical genetics : BJMG · 2021
    Article
  3. Auditory phenotype of Smith-Lemli-Opitz syndrome.American journal of medical genetics. Part A · 2021
    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

13 authors at 6 institutions in 2 countries.

Yasemen ErogluDepartment of Pediatrics, Oregon Health and Science University, Portland, Oregon.ORCID http://orcid.org/0000-0002-7874-7003
Mina Nguyen-DriverDepartment of Pediatrics, Oregon Health and Science University, Portland, Oregon.
Robert D SteinerDepartment of Pediatrics, Oregon Health and Science University, Portland, Oregon.
Louise MerkensDepartment of Pediatrics, Oregon Health and Science University, Portland, Oregon.
Mark MerkensDepartment of Pediatrics, Oregon Health and Science University, Portland, Oregon.
Jean-Baptiste RoulletDepartment of Pediatrics, Oregon Health and Science University, Portland, Oregon.
Ellen EliasChildren's Hospital Colorado, Aurora, Colorado.
Geeta SarphareKennedy Krieger Institute, Baltimore, Maryland.
Forbes D PorterProgram in Developmental Endocrinology and Genetics, Eunice Kennedy Shriver National Institution of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland.
Chumei LiDepartment of Pathology and Medicine, and Pediatrics, McMaster University, Hamilton, ON, Canada.
Elaine TierneyKennedy Krieger Institute, Baltimore, Maryland.
Małgorzata J NowaczykDepartment of Pathology and Medicine, and Pediatrics, McMaster University, Hamilton, ON, Canada.
Kurt A FreemanDepartment of Pediatrics, Oregon Health and Science University, Portland, Oregon.
Oregon Health & Science University · USKennedy Krieger Institute · USMcMaster University · CAChildren's Hospital Colorado · USNational Institutes of Health · USUniversity of Wisconsin–Madison · US

Funding

Sterol and Isoprenoid Diseases Consortium Supplement 2018U54HD061939 · NICHD · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI RIZZO, WILLIAM B. · 2009 to 2018
$6.6M
Dietary Cholesterol and Defects in Cholesterol SynthesisR01HL073980 · NHLBI · OREGON HEALTH & SCIENCE UNIVERSITY · PI STEINER, ROBERT DAVID · 2003 to 2013
$4.5M
Clinical Investigations of Smith-Lemli-Opitz SyndromeZIAHD008825 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI PORTER, FORBES · 2009 to 2019
$2.2M
2016 International Conference on Plant Sterols, Health & DiseasesR13AT009270 · NCCIH · WASHINGTON STATE UNIVERSITY · PI ROULLET, JEAN-BAPTISTE O · 2016 to 2016
$40k
NCCIH NIH HHS R13 AT009270NHLBI NIH HHS R01 HL073980NICHD NIH HHS U54 HD061939
6 · The paper itself

Abstract

Children with Smith-Lemli-Opitz syndrome (SLOS) are typically reported to have moderate to severe intellectual disability. This study aims to determine whether normal cognitive function is possible in this population and to describe clinical, biochemical and molecular characteristics of children with SLOS and normal intelligent quotient (IQ). The study included children with SLOS who underwent cognitive testing in four centers. All children with at least one IQ composite score above 80 were included in the study. Six girls, three boys with SLOS were found to have normal or low-normal IQ in a cohort of 145 children with SLOS. Major/multiple organ anomalies and low serum cholesterol levels were uncommon. No correlation with IQ and genotype was evident and no specific developmental profile were observed. Thus, normal or low-normal cognitive function is possible in SLOS. Further studies are needed to elucidate factors contributing to normal or low-normal cognitive function in children with SLOS.

Indexed as

Abnormalities, MultipleAdolescentChildChild, PreschoolCognitionFemaleGenotypeHumansInfantInfant, NewbornIntelligence TestsMaleOxidoreductases Acting on CH-CH Group DonorsSmith-Lemli-Opitz Syndrome7-dehydrocholesterol reductaseOxidoreductases Acting on CH-CH Group DonorsdevelopmentIQSmith-Lemli-Opitz

Identifiers

PMID28349652
PMCPMC6016830
OpenAlexW2603562387

What OpenQuestion holds

Textmetadata
LicenceTDM
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.