Literature DB >> 30968316

Autism Spectrum Disorder and Psychiatric Comorbidity in a Patient with Myhre Syndrome.

Pehlivanidis Artemios1, Spyropoulou Areti2, Papanikolaou Katerina3, Fryssira Helen4, Tsoytsoy Eirini4, Papageorgiou Charalambos2.   

Abstract

Myhre syndrome (MS) is a connective tissue disorder with multisystem involvement with or without intellectual disability. In most cases SMAD4 mutations are reported. To date, 55 individuals have been molecularly confirmed. Autism has been proposed among associate clinical features of MS but no standardized diagnosis was available in previous cases. We report a case of a 25-year-old man with a pathogenic heterozygous SMAD4 missense mutation affecting residue Arg496 (SMAD4:p.Arg496Cys). Clinical findings are consistent with MS, commorbid with affective disorder and High Functioning Autism Spectrum Disorder confirmed by a standardized assessment procedure. The thorough clinical assessment of cases with syndromes such as MS can extend our knowledge on both the phenotypic characteristics of the syndrome and the genetic basis of autism.

Entities:  

Keywords:  Affective disorder; High functioning autism spectrum disorder; Myhre syndrome; SMAD4 mutation

Mesh:

Substances:

Year:  2019        PMID: 30968316     DOI: 10.1007/s10803-019-04015-y

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


  13 in total

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Journal:  J Med Genet       Date:  2003-07       Impact factor: 6.318

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Journal:  Clin Genet       Date:  1981-07       Impact factor: 4.438

3.  Novel SMAD4 mutation causing Myhre syndrome.

Authors:  Viviana Caputo; Gianfranco Bocchinfuso; Marco Castori; Alice Traversa; Antonio Pizzuti; Lorenzo Stella; Paola Grammatico; Marco Tartaglia
Journal:  Am J Med Genet A       Date:  2014-04-08       Impact factor: 2.802

4.  Clinical and mutational spectrum in a cohort of 105 unrelated patients with dilated cardiomyopathy.

Authors:  Gilles Millat; Patrice Bouvagnet; Philippe Chevalier; Laurent Sebbag; Arnaud Dulac; Claire Dauphin; Pierre-Simon Jouk; Marie-Ange Delrue; Jean-Benoit Thambo; Philippe Le Metayer; Marie-France Seronde; Laurence Faivre; Jean-Christophe Eicher; Robert Rousson
Journal:  Eur J Med Genet       Date:  2011-08-04       Impact factor: 2.708

5.  Self and informant reports of mental health difficulties among adults with autism findings from a long-term follow-up study.

Authors:  Philippa Moss; Patricia Howlin; Sarah Savage; Patrick Bolton; Michael Rutter
Journal:  Autism       Date:  2015-05-26

6.  Spatial Clustering of de Novo Missense Mutations Identifies Candidate Neurodevelopmental Disorder-Associated Genes.

Authors:  Stefan H Lelieveld; Laurens Wiel; Hanka Venselaar; Rolph Pfundt; Gerrit Vriend; Joris A Veltman; Han G Brunner; Lisenka E L M Vissers; Christian Gilissen
Journal:  Am J Hum Genet       Date:  2017-08-31       Impact factor: 11.025

7.  Myhre and LAPS syndromes: clinical and molecular review of 32 patients.

Authors:  Caroline Michot; Carine Le Goff; Clémentine Mahaut; Alexandra Afenjar; Alice S Brooks; Philippe M Campeau; Anne Destree; Maja Di Rocco; Dian Donnai; Raoul Hennekam; Delphine Heron; Sébastien Jacquemont; Peter Kannu; Angela E Lin; Sylvie Manouvrier-Hanu; Sahar Mansour; Sandrine Marlin; Ruth McGowan; Helen Murphy; Annick Raas-Rothschild; Marlène Rio; Marleen Simon; Irene Stolte-Dijkstra; James R Stone; Yves Sznajer; John Tolmie; Renaud Touraine; Jenneke van den Ende; Nathalie Van der Aa; Ton van Essen; Alain Verloes; Arnold Munnich; Valérie Cormier-Daire
Journal:  Eur J Hum Genet       Date:  2014-01-15       Impact factor: 4.246

8.  Common genetic variants contribute to risk of rare severe neurodevelopmental disorders.

Authors:  Mari E K Niemi; Hilary C Martin; Daniel L Rice; Giuseppe Gallone; Scott Gordon; Martin Kelemen; Kerrie McAloney; Jeremy McRae; Elizabeth J Radford; Sui Yu; Jozef Gecz; Nicholas G Martin; Caroline F Wright; David R Fitzpatrick; Helen V Firth; Matthew E Hurles; Jeffrey C Barrett
Journal:  Nature       Date:  2018-09-26       Impact factor: 49.962

9.  Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains.

Authors:  Madeleine R Geisheker; Gabriel Heymann; Tianyun Wang; Bradley P Coe; Tychele N Turner; Holly A F Stessman; Kendra Hoekzema; Malin Kvarnung; Marie Shaw; Kathryn Friend; Jan Liebelt; Christopher Barnett; Elizabeth M Thompson; Eric Haan; Hui Guo; Britt-Marie Anderlid; Ann Nordgren; Anna Lindstrand; Geert Vandeweyer; Antonino Alberti; Emanuela Avola; Mirella Vinci; Stefania Giusto; Tiziano Pramparo; Karen Pierce; Srinivasa Nalabolu; Jacob J Michaelson; Zdenek Sedlacek; Gijs W E Santen; Hilde Peeters; Hakon Hakonarson; Eric Courchesne; Corrado Romano; R Frank Kooy; Raphael A Bernier; Magnus Nordenskjöld; Jozef Gecz; Kun Xia; Larry S Zweifel; Evan E Eichler
Journal:  Nat Neurosci       Date:  2017-06-19       Impact factor: 24.884

10.  A restricted spectrum of mutations in the SMAD4 tumor-suppressor gene underlies Myhre syndrome.

Authors:  Viviana Caputo; Luciano Cianetti; Marcello Niceta; Claudio Carta; Andrea Ciolfi; Gianfranco Bocchinfuso; Eugenio Carrani; Maria Lisa Dentici; Elisa Biamino; Elga Belligni; Livia Garavelli; Loredana Boccone; Daniela Melis; Generoso Andria; Bruce D Gelb; Lorenzo Stella; Margherita Silengo; Bruno Dallapiccola; Marco Tartaglia
Journal:  Am J Hum Genet       Date:  2012-01-13       Impact factor: 11.025

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  5 in total

1.  Novel Ocular and Inner Ear Anomalies in a Patient with Myhre Syndrome.

Authors:  Semra Gürsoy; Filiz Hazan; Tülay Öztürk; Halil Ateş
Journal:  Mol Syndromol       Date:  2019-12-20

2.  Analysis of Faecal Microbiota and Small ncRNAs in Autism: Detection of miRNAs and piRNAs with Possible Implications in Host-Gut Microbiota Cross-Talk.

Authors:  Federica Chiappori; Francesca Anna Cupaioli; Arianna Consiglio; Noemi Di Nanni; Ettore Mosca; Vito Flavio Licciulli; Alessandra Mezzelani
Journal:  Nutrients       Date:  2022-03-23       Impact factor: 5.717

3.  Natural history of Myhre syndrome.

Authors:  David Dawei Yang; Marlene Rio; Caroline Michot; Nathalie Boddaert; Wael Yacoub; Nicolas Garcelon; Briac Thierry; Damien Bonnet; Sophie Rondeau; Dominique Herve; Stephanie Guey; Francois Angoulvant; Valerie Cormier-Daire
Journal:  Orphanet J Rare Dis       Date:  2022-07-30       Impact factor: 4.303

4.  Gene expression changes associated with trajectories of psychopathology in a longitudinal cohort of children and adolescents.

Authors:  Vanessa Kiyomi Ota; Marcos Leite Santoro; Leticia Maria Spindola; Pedro Mario Pan; Andressa Simabucuro; Gabriela Xavier; Tamiris Vieira-Fonseca; Evelin Aline Zanardo; Felipe Rodolfo Camargo Dos Santos; Julia Luiza Schäfer; Leslie Domenici Kulikowski; Pedro A F Galante; Paula Fontes Asprino; Elisa Brietzke; Rodrigo Grassi-Oliveira; Luis Augusto Rohde; Euripedes Constantino Miguel; Ary Gadelha; Jair Jesus Mari; Rodrigo Affonseca Bressan; Giovanni Abrahao Salum; Sintia Iole Belangero
Journal:  Transl Psychiatry       Date:  2020-03-17       Impact factor: 6.222

Review 5.  Does the Arc of Science Bend Towards Impact? Four Decades of Empirical Research Published in JADD Since the DSM-III.

Authors:  Peter Doehring
Journal:  J Autism Dev Disord       Date:  2021-05-11
  5 in total

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