Literature DB >> 33727758

Co-occurring medical conditions among individuals with ASD-associated disruptive mutations.

Evangeline C Kurtz-Nelson1, Jennifer S Beighley1, Caitlin M Hudac2, Jennifer Gerdts1, Arianne S Wallace1, Kendra Hoekzema3, Evan E Eichler3,4, Raphael A Bernier1.   

Abstract

Children with autism spectrum disorder (ASD) are at risk for co-occurring medical conditions, many of which have also been reported among individuals with mutations in ASD-associated genes. This study examined rates of co-occurring medical conditions across 301 individuals with disruptive mutations to 1 of 18 ASD-risk genes in comparison to rates of conditions in an idiopathic ASD sample. Rates of gastrointestinal problems, seizures, physical anomalies, and immune problems were generally elevated, with significant differences in rates observed between groups. Results may inform medical care of individuals with ASD-associated mutations and research into mechanisms of co-occurring medical conditions in ASD.

Entities:  

Year:  2020        PMID: 33727758      PMCID: PMC7958308          DOI: 10.1080/02739615.2020.1741361

Source DB:  PubMed          Journal:  Child Health Care        ISSN: 0273-9615


  69 in total

1.  Is MED13L-related intellectual disability a recognizable syndrome?

Authors:  Pernille Mathiesen Tørring; Martin Jakob Larsen; Charlotte Brasch-Andersen; Lotte Nylandsted Krogh; Maria Kibæk; Lone Laulund; Niels Illum; Ulrike Dunkhase-Heinl; Antje Wiesener; Bernt Popp; Giuseppe Marangi; Tina Duelund Hjortshøj; Jakob Ek; Ida Vogel; Naja Becher; Laura Roos; Marcella Zollino; Christina Ringmann Fagerberg
Journal:  Eur J Med Genet       Date:  2018-06-27       Impact factor: 2.708

2.  Clustering of co-occurring conditions in autism spectrum disorder during early childhood: A retrospective analysis of medical claims data.

Authors:  Troy Vargason; Richard E Frye; Deborah L McGuinness; Juergen Hahn
Journal:  Autism Res       Date:  2019-05-31       Impact factor: 5.216

Review 3.  Genetics of autism spectrum disorder.

Authors:  Gokul Ramaswami; Daniel H Geschwind
Journal:  Handb Clin Neurol       Date:  2018

Review 4.  The state of research on the genetics of autism spectrum disorder: methodological, clinical and conceptual progress.

Authors:  Anne B Arnett; Sandy Trinh; Raphael A Bernier
Journal:  Curr Opin Psychol       Date:  2018-07-21

5.  Dietary fibre intake and constipation in children with severe developmental disabilities.

Authors:  P W Tse; S S Leung; T Chan; A Sien; A K Chan
Journal:  J Paediatr Child Health       Date:  2000-06       Impact factor: 1.954

6.  Genotype-phenotype evaluation of MED13L defects in the light of a novel truncating and a recurrent missense mutation.

Authors:  Reza Asadollahi; Markus Zweier; Laura Gogoll; Raphael Schiffmann; Heinrich Sticht; Katharina Steindl; Anita Rauch
Journal:  Eur J Med Genet       Date:  2017-06-21       Impact factor: 2.708

7.  Otitis Media and Related Complications Among Children with Autism Spectrum Disorders.

Authors:  Daniel J Adams; Apryl Susi; Christine R Erdie-Lalena; Gregory Gorman; Elizabeth Hisle-Gorman; Michael Rajnik; Marilisa Elrod; Cade M Nylund
Journal:  J Autism Dev Disord       Date:  2016-05

8.  Recurrent otitis media in the fragile X syndrome.

Authors:  R J Hagerman; D Altshul-Stark; P McBogg
Journal:  Am J Dis Child       Date:  1987-02

9.  Structural analysis of pathogenic mutations in the DYRK1A gene in patients with developmental disorders.

Authors:  Jochem M G Evers; Roman A Laskowski; Marta Bertolli; Jill Clayton-Smith; Charu Deshpande; Jacqueline Eason; Frances Elmslie; Frances Flinter; Carol Gardiner; Jane A Hurst; Helen Kingston; Usha Kini; Anne K Lampe; Derek Lim; Alison Male; Swati Naik; Michael J Parker; Sue Price; Leema Robert; Ajoy Sarkar; Volker Straub; Geoff Woods; Janet M Thornton; Caroline F Wright
Journal:  Hum Mol Genet       Date:  2017-02-01       Impact factor: 6.150

10.  Clinical Presentation of a Complex Neurodevelopmental Disorder Caused by Mutations in ADNP.

Authors:  Anke Van Dijck; Anneke T Vulto-van Silfhout; Elisa Cappuyns; Ilse M van der Werf; Grazia M Mancini; Andreas Tzschach; Raphael Bernier; Illana Gozes; Evan E Eichler; Corrado Romano; Anna Lindstrand; Ann Nordgren; Malin Kvarnung; Tjitske Kleefstra; Bert B A de Vries; Sébastien Küry; Jill A Rosenfeld; Marije E Meuwissen; Geert Vandeweyer; R Frank Kooy
Journal:  Biol Psychiatry       Date:  2018-03-15       Impact factor: 13.382

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  2 in total

1.  Whole-genome sequencing combined RNA-sequencing analysis of patients with mutations in SET binding protein 1.

Authors:  Li Liu; Xiaoshu Feng; Sihan Liu; Yanqiu Zhou; Xiaojing Dong; Hong Yao; Bo Tan
Journal:  Front Neurosci       Date:  2022-09-07       Impact factor: 5.152

2.  Brief Report: Associations Between Self-injurious Behaviors and Abdominal Pain Among Individuals with ASD-Associated Disruptive Mutations.

Authors:  Evangeline C Kurtz-Nelson; See Wan Tham; Kaitlyn Ahlers; Daniel Cho; Arianne S Wallace; Evan E Eichler; Raphael A Bernier; Rachel K Earl
Journal:  J Autism Dev Disord       Date:  2020-11-11
  2 in total

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