Literature DB >> 22089167

Diagnostic yield of chromosomal microarray analysis in an autism primary care practice: which guidelines to implement?

Susan G McGrew1, Brittany R Peters, Julie A Crittendon, Jeremy Veenstra-Vanderweele.   

Abstract

Genetic testing is recommended for patients with ASD; however specific recommendations vary by specialty. American Academy of Pediatrics and American Academy of Neurology guidelines recommend G-banded karyotype and Fragile X DNA. The American College of Medical Genetics recommends Chromosomal Microarray Analysis (CMA). We determined the yield of CMA (N = 85), karyotype (N = 119), and fragile X (N = 174) testing in a primary pediatrics autism practice. We found twenty (24%) patients with abnormal CMA results (eight were clinically significant), three abnormal karyotypes and one Fragile X syndrome. There was no relationship between CMA result and cognitive level, seizures, dysmorphology, congenital malformations or behavior. We conclude that CMA should be the clinical standard in all specialties for first tier genetic testing in ASD.

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Year:  2012        PMID: 22089167     DOI: 10.1007/s10803-011-1398-3

Source DB:  PubMed          Journal:  J Autism Dev Disord        ISSN: 0162-3257


  56 in total

1.  A case with de novo interstitial deletion of chromosome 7q21.1-q22.

Authors:  E Manguoğlu; S Berker-Karaüzüm; A Baumer; E Mihçi; S Taçoy; G Lüleci; A Schinzel
Journal:  Genet Couns       Date:  2005

2.  Behavior checklist for identifying severely handicapped individuals with high levels of autistic behavior.

Authors:  D A Krug; J Arick; P Almond
Journal:  J Child Psychol Psychiatry       Date:  1980-07       Impact factor: 8.982

3.  The autism diagnostic observation schedule-generic: a standard measure of social and communication deficits associated with the spectrum of autism.

Authors:  C Lord; S Risi; L Lambrecht; E H Cook; B L Leventhal; P C DiLavore; A Pickles; M Rutter
Journal:  J Autism Dev Disord       Date:  2000-06

Review 4.  Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.

Authors:  David T Miller; Margaret P Adam; Swaroop Aradhya; Leslie G Biesecker; Arthur R Brothman; Nigel P Carter; Deanna M Church; John A Crolla; Evan E Eichler; Charles J Epstein; W Andrew Faucett; Lars Feuk; Jan M Friedman; Ada Hamosh; Laird Jackson; Erin B Kaminsky; Klaas Kok; Ian D Krantz; Robert M Kuhn; Charles Lee; James M Ostell; Carla Rosenberg; Stephen W Scherer; Nancy B Spinner; Dimitri J Stavropoulos; James H Tepperberg; Erik C Thorland; Joris R Vermeesch; Darrel J Waggoner; Michael S Watson; Christa Lese Martin; David H Ledbetter
Journal:  Am J Hum Genet       Date:  2010-05-14       Impact factor: 11.025

5.  Clinical and molecular characterization of individuals with 18p deletion: a genotype-phenotype correlation.

Authors:  Ulrika Wester; Marie-Louise Bondeson; Christina Edeby; Göran Annerén
Journal:  Am J Med Genet A       Date:  2006-06-01       Impact factor: 2.802

6.  A complex chromosome 7q rearrangement identified in a patient with mental retardation, anxiety disorder, and autistic features.

Authors:  Johannes G Dauwerse; Claudia A Ruivenkamp; Kerstin Hansson; Godfried M Marijnissen; Dorien J M Peters; Martijn H Breuning; Yvonne Hilhorst-Hofstee
Journal:  Am J Med Genet A       Date:  2010-02       Impact factor: 2.802

7.  Genetic and clinical characterization of patients with an interstitial duplication 15q11-q13, emphasizing behavioral phenotype and response to treatment.

Authors:  J A Thomas; J Johnson; T L Peterson Kraai; R Wilson; N Tartaglia; J LeRoux; L Beischel; L McGavran; R J Hagerman
Journal:  Am J Med Genet A       Date:  2003-06-01       Impact factor: 2.802

8.  10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequences.

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Journal:  Cytogenet Genome Res       Date:  2009-04-15       Impact factor: 1.636

9.  Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder.

Authors:  Susan L Christian; Camille W Brune; Jyotsna Sudi; Ravinesh A Kumar; Shaung Liu; Samer Karamohamed; Judith A Badner; Seiichi Matsui; Jeffrey Conroy; Devin McQuaid; James Gergel; Eli Hatchwell; T Conrad Gilliam; Elliot S Gershon; Norma J Nowak; William B Dobyns; Edwin H Cook
Journal:  Biol Psychiatry       Date:  2008-03-28       Impact factor: 13.382

Review 10.  Autistic phenotypes and genetic testing: state-of-the-art for the clinical geneticist.

Authors:  C Lintas; A M Persico
Journal:  J Med Genet       Date:  2008-08-26       Impact factor: 6.318

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  21 in total

1.  Autism in association with Triple X syndrome.

Authors:  Syed Irfan Ali; Nollaig Byrne; Aisling Mulligan
Journal:  Eur Child Adolesc Psychiatry       Date:  2012-02-04       Impact factor: 4.785

2.  Children with 7q11.23 duplication syndrome: psychological characteristics.

Authors:  Carolyn B Mervis; Bonita P Klein-Tasman; Myra J Huffman; Shelley L Velleman; C Holley Pitts; Danielle R Henderson; Janet Woodruff-Borden; Colleen A Morris; Lucy R Osborne
Journal:  Am J Med Genet A       Date:  2015-04-21       Impact factor: 2.802

3.  Autism Spectrum Symptomatology Among Children with Duplication 7q11.23 Syndrome.

Authors:  Bonita P Klein-Tasman; Carolyn B Mervis
Journal:  J Autism Dev Disord       Date:  2018-06

4.  7q11.23 Duplication syndrome: Physical characteristics and natural history.

Authors:  Colleen A Morris; Carolyn B Mervis; Alex P Paciorkowski; Omar Abdul-Rahman; Sarah L Dugan; Alan F Rope; Patricia Bader; Laura G Hendon; Shelley L Velleman; Bonita P Klein-Tasman; Lucy R Osborne
Journal:  Am J Med Genet A       Date:  2015-09-03       Impact factor: 2.802

5.  Genetic testing and genetic counseling among Medicaid-enrolled children with autism spectrum disorder in 2001 and 2007.

Authors:  Lindsay Shea; Craig J Newschaffer; Ming Xie; Scott M Myers; David S Mandell
Journal:  Hum Genet       Date:  2013-09-15       Impact factor: 4.132

6.  Impact of acamprosate on plasma amyloid-β precursor protein in youth: a pilot analysis in fragile X syndrome-associated and idiopathic autism spectrum disorder suggests a pharmacodynamic protein marker.

Authors:  Craig A Erickson; Balmiki Ray; Bryan Maloney; Logan K Wink; Katherine Bowers; Tori L Schaefer; Christopher J McDougle; Deborah K Sokol; Debomoy K Lahiri
Journal:  J Psychiatr Res       Date:  2014-08-19       Impact factor: 4.791

7.  What Do Parents Think about Chromosomal Microarray Testing? A Qualitative Report from Parents of Children with Autism Spectrum Disorders.

Authors:  Lei Xu; Linda Crane Mitchell; Alice R Richman; Kaitlyn Clawson
Journal:  Autism Res Treat       Date:  2016-06-20

8.  Clinical Performance of an Ultrahigh Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders.

Authors:  Karen S Ho; Hope Twede; Rena Vanzo; Erin Harward; Charles H Hensel; Megan M Martin; Stephanie Page; Andreas Peiffer; Patricia Mowery-Rushton; Moises Serrano; E Robert Wassman
Journal:  Biomed Res Int       Date:  2016-11-16       Impact factor: 3.411

9.  Capturing the clinical utility of genomic testing: medical recommendations following pediatric microarray.

Authors:  Robin Z Hayeems; Ny Hoang; Sebastien Chenier; Dimitri J Stavropoulos; Shuye Pu; Rosanna Weksberg; Cheryl Shuman
Journal:  Eur J Hum Genet       Date:  2014-12-10       Impact factor: 4.246

Review 10.  Genetic Counseling for Autism Spectrum Disorder in an Evolving Theoretical Landscape.

Authors:  Brenda Finucane; Scott M Myers
Journal:  Curr Genet Med Rep       Date:  2016-06-24
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