Evidence map›Paper›PMID 32954672›Full record

ArticleAmerican journal of medical genetics. Part A2021

Neurocognitive, adaptive, and psychosocial functioning in individuals with Robinow syndrome.

David D Schwartz, Rachel H Fein, Claudia M B Carvalho, V Reid Sutton, Juliana F Mazzeu, Marni E Axelrad

Abstract read
In one paragraph

Article in American journal of medical genetics. Part A, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.4field-weighted citation impact, top 39% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

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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

6 authors at 2 institutions in 2 countries.

David D SchwartzSection of Psychology, Department of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.ORCID 0000-0002-4461-0914
Rachel H FeinSection of Psychology, Department of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.ORCID 0000-0002-1004-167X
Claudia M B CarvalhoDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.ORCID 0000-0002-2090-298X
V Reid SuttonDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.ORCID 0000-0002-6450-8554
Juliana F MazzeuFaculty of Medicine, Universidade de Brasília, Brasília, Brazil.ORCID 0000-0002-6161-0510
Marni E AxelradSection of Psychology, Department of Pediatrics, Baylor College of Medicine, Houston, Texas, USA.ORCID 0000-0002-8865-971X
Baylor College of Medicine · USUniversidade de Brasília · BR

Funding

Discovery and functional characterization of genic variants leading to Robinow syndrome and related skeletal dysplasias.R03HD092569 · NICHD · BAYLOR COLLEGE OF MEDICINE · PI FONSECA, CLAUDIA CARVALHO, SUTTON, VERNON R · 2018 to 2019
$238k
NICHD NIH HHS R03 HD092569
6 · The paper itself

Abstract

It has been estimated that 10-15% of people with Robinow syndrome (RS) show delayed development, but no studies have formally assessed developmental domains. The objective of this study is to provide the first description of cognitive, adaptive, and psychological functioning in RS. Thirteen participants (10 males) aged 4-51 years were seen for neuropsychological screening. Eight had autosomal-dominant RS (DVL1, n = 5; WNT5A, n = 3), four had autosomal-recessive RS (NXN, n = 2; ROR2, n = 2), and one had a mutation on an RS candidate gene (GPC4). Participants completed measures of intellectual, fine-motor, adaptive, executive, and psychological functioning. Findings indicated generally average intellectual functioning and low-average visuomotor skills. Adaptive functioning was average in autosomal-recessive RS (RRS) but low average in autosomal-dominant RS (DRS). Parent-report indicated executive dysfunction and attention problems in 4/8 children, 3/4 of whom had a DVL1 variant; adult self-report did not indicate similar difficulties. Learning disabilities were also reported in 4/8 individuals with DRS, 3/4 of whom had a DVL1 variant. Peer problems were reported for a majority of participants, many of whom also reported emotional concerns. Altogether, the findings indicate average neurocognitive functioning in RRS. In contrast, DRS, especially DVL1 pathogenic alleles, may confer specific risk for neurodevelopmental disability.

Indexed as

AdolescentAdultAllelesChildChild, PreschoolCraniofacial AbnormalitiesDevelopmental DisabilitiesDishevelled ProteinsDwarfismGenetic Predisposition to DiseaseHumansLearning DisabilitiesLimb Deformities, CongenitalMaleMiddle AgedNeurocognitive DisordersDishevelled ProteinsDVL1 protein, humanWnt-5a ProteinWNT5A protein, humanadaptivecognitivepsychologicalRobinow syndromesocial

Identifiers

PMID32954672
PMCPMC13619162
OpenAlexW3087512308

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.