Literature DB >> 18197051

Genetics evaluation for the etiologic diagnosis of autism spectrum disorders.

G Bradley Schaefer1, Nancy J Mendelsohn.   

Abstract

Over the past decade, the reported incidence of autism spectrum disorders has continued to increase. Coincident with this, the number of referrals to clinical geneticists to identify the etiology has also dramatically increased. The reported diagnostic yield for autism spectrum disorders is commonly reported in the range of 6-15%. However, continued advances in genetic technology expand the diagnostic options available for these evaluations and presumably increase the diagnostic yield. The list of genetic and metabolic conditions that have been reported with an autism phenotype is quite extensive. In deciding on an evaluation plan, the clinical geneticist has the difficult task of balancing an ever-expanding list of available tests and possible diagnoses with the issues of cost, practicality, and expected yield. In this article, we discuss a strategy of a tiered evaluation of the etiology of autism. These recommendations use evidence-based conclusions from the current available literature and cumulative clinical experience.

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Mesh:

Year:  2008        PMID: 18197051     DOI: 10.1097/GIM.0b013e31815efdd7

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  46 in total

Review 1.  Genetics in child and adolescent psychiatry: methodological advances and conceptual issues.

Authors:  Sarah Hohmann; Nicoletta Adamo; Benjamin B Lahey; Stephen V Faraone; Tobias Banaschewski
Journal:  Eur Child Adolesc Psychiatry       Date:  2015-04-08       Impact factor: 4.785

Review 2.  Mitochondrial dysfunction can connect the diverse medical symptoms associated with autism spectrum disorders.

Authors:  Richard E Frye; Daniel A Rossignol
Journal:  Pediatr Res       Date:  2011-05       Impact factor: 3.756

Review 3.  Autism.

Authors:  Susan E Levy; David S Mandell; Robert T Schultz
Journal:  Lancet       Date:  2009-10-12       Impact factor: 79.321

Review 4.  Disentangling the heterogeneity of autism spectrum disorder through genetic findings.

Authors:  Shafali S Jeste; Daniel H Geschwind
Journal:  Nat Rev Neurol       Date:  2014-01-28       Impact factor: 42.937

5.  FORWARD: A Registry and Longitudinal Clinical Database to Study Fragile X Syndrome.

Authors:  Stephanie L Sherman; Sharon A Kidd; Catharine Riley; Elizabeth Berry-Kravis; Howard F Andrews; Robert M Miller; Sharyn Lincoln; Mark Swanson; Walter E Kaufmann; W Ted Brown
Journal:  Pediatrics       Date:  2017-06       Impact factor: 7.124

6.  Copy Number Variants and Polygenic Risk Scores Predict Need of Care in Autism and/or ADHD Families.

Authors:  Sonja LaBianca; Jette LaBianca; Anne Katrine Pagsberg; Klaus Damgaard Jakobsen; Vivek Appadurai; Alfonso Buil; Thomas Werge
Journal:  J Autism Dev Disord       Date:  2021-01

7.  Pre-eclampsia, birth weight, and autism spectrum disorders.

Authors:  Joshua R Mann; Suzanne McDermott; Haikun Bao; James Hardin; Anthony Gregg
Journal:  J Autism Dev Disord       Date:  2010-05

Review 8.  Syndromic autism: causes and pathogenetic pathways.

Authors:  Arianna Benvenuto; Romina Moavero; Riccardo Alessandrelli; Barbara Manzi; Paolo Curatolo
Journal:  World J Pediatr       Date:  2009-08-20       Impact factor: 2.764

Review 9.  Fragile X syndrome: A review of clinical management.

Authors:  Reymundo Lozano; Atoosa Azarang; Tanaporn Wilaisakditipakorn; Randi J Hagerman
Journal:  Intractable Rare Dis Res       Date:  2016-08

10.  Recent advances in the pathogenesis of syndromic autisms.

Authors:  A Benvenuto; B Manzi; R Alessandrelli; C Galasso; P Curatolo
Journal:  Int J Pediatr       Date:  2009-06-21
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