Literature DB >> 30919832

Evaluation of the child with global developmental delay and intellectual disability.

Stacey A Bélanger1, Joannie Caron1.   

Abstract

Global developmental delay (GDD) and intellectual disability (ID) are common concerns in the paediatric setting. Etiologies of both conditions are highly heterogeneous. The American Academy of Pediatrics, the American Academy of Neurology and the British Columbia-based Treatable Intellectual Disability Endeavor (TIDE) protocol have each proposed multitiered investigations of GDD/ID to guide physicians toward an understanding of etiology that optimizes therapeutic yield. This statement provides a framework for the clinical investigation of GDD/ID in children, along with an updated protocol for Canadian physicians to follow in the etiological investigation of GDD/ID. The revised protocol is based on current knowledge and existing guidelines. Key elements of investigation include formal vision and hearing testing, chromosomal microarray, Fragile-X DNA testing and first-tier testing for treatable inborn errors of metabolism. Brain imaging is recommended in the presence of specific neurological findings.

Entities:  

Keywords:  Chromosome microarray; Global developmental delay; IEM; Intellectual disability

Year:  2018        PMID: 30919832      PMCID: PMC6234423          DOI: 10.1093/pch/pxy093

Source DB:  PubMed          Journal:  Paediatr Child Health        ISSN: 1205-7088            Impact factor:   2.253


  20 in total

1.  Caring for children with mental health or developmental and behavioural disorders: Perspectives of family health teams on roles and barriers to care.

Authors:  Elizabeth Young; Laurie Green; Rachel Goldfarb; Kathleen Hollamby; Karen Milligan
Journal:  Can Fam Physician       Date:  2020-10       Impact factor: 3.275

2.  Diagnostic yield from routine metabolic screening tests in evaluation of global developmental delay and intellectual disability.

Authors:  Hilary Vallance; Graham Sinclair; Bojana Rakic; Sylvia Stockler-Ipsiroglu
Journal:  Paediatr Child Health       Date:  2020-12-19       Impact factor: 2.253

Review 3.  Follow-up care of the extremely preterm infant after discharge from the neonatal intensive care unit.

Authors:  Leonora Hendson; Paige T Church; Rudaina Banihani
Journal:  Paediatr Child Health       Date:  2022-10-03       Impact factor: 2.600

Review 4.  Standards of diagnostic assessment for autism spectrum disorder.

Authors:  Jessica A Brian; Lonnie Zwaigenbaum; Angie Ip
Journal:  Paediatr Child Health       Date:  2019-10-24       Impact factor: 2.253

5.  Utility of metabolic screening in neurological presentations of infancy.

Authors:  Djurdja Djordjevic; Etsuko Tsuchiya; Megan Fitzpatrick; Neal Sondheimer; James J Dowling
Journal:  Ann Clin Transl Neurol       Date:  2020-06-04       Impact factor: 4.511

Review 6.  Treatable inherited metabolic disorders causing intellectual disability: 2021 review and digital app.

Authors:  Eva M M Hoytema van Konijnenburg; Saskia B Wortmann; Marina J Koelewijn; Laura A Tseng; Roderick Houben; Sylvia Stöckler-Ipsiroglu; Carlos R Ferreira; Clara D M van Karnebeek
Journal:  Orphanet J Rare Dis       Date:  2021-04-12       Impact factor: 4.123

7.  Use of the Griffiths mental development scale-Chinese in the assessment of children with autism spectrum disorder and global developmental delay/intellectual disability.

Authors:  Hui Wang; Yu Du; Zhenghuan Mao; Yueping Che; Haifeng Li; Li Ding; Huiying Jin
Journal:  Medicine (Baltimore)       Date:  2021-04-02       Impact factor: 1.817

Review 8.  Calcium channelopathies and intellectual disability: a systematic review.

Authors:  Miriam Kessi; Baiyu Chen; Jing Peng; Fangling Yan; Lifen Yang; Fei Yin
Journal:  Orphanet J Rare Dis       Date:  2021-05-13       Impact factor: 4.123

9.  Genome-Wide Sequencing for Unexplained Developmental Disabilities or Multiple Congenital Anomalies: A Health Technology Assessment.

Authors: 
Journal:  Ont Health Technol Assess Ser       Date:  2020-03-06

10.  Next-generation gene panel testing in adolescents and adults in a medical neuropsychiatric genetics clinic.

Authors:  Y Trakadis; A Accogli; B Qi; D Bloom; R Joober; E Levy; K Tabbane
Journal:  Neurogenetics       Date:  2021-08-07       Impact factor: 2.660

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