Literature DB >> 12664274

A case of autism in a child with Apert's syndrome.

Jaime Morey-Canellas1, U Sivagamasundari, Hilary Barton.   

Abstract

We present the case of a 7-year-old child with Aspert's syndrome who was diagnosed as suffering from childhood autism. As far as we are aware this is the first described association between autism and acrocephalosyndactyly syndromes. We discuss issues regarding the diagnosis and co-morbidity of the autistic spectrum disorders.

Entities:  

Mesh：

Year:  2003        PMID： 12664274     DOI： 10.1007/s00787-003-0289-3

Source DB:  PubMed          Journal:  Eur Child Adolesc Psychiatry        ISSN： 1018-8827            Impact factor:   4.785


  4 in total

1.  A case report of two male siblings with autism and duplication of Xq13-q21, a region including three genes predisposing for autism.

Authors:  Elisabet Wentz; Mihailo Vujic; Ewa-Lotta Kärrstedt; Anna Erlandsson; Christopher Gillberg
Journal:  Eur Child Adolesc Psychiatry       Date:  2013-08-23       Impact factor: 4.785

2.  NEGR1 and FGFR2 cooperatively regulate cortical development and core behaviours related to autism disorders in mice.

Authors:  Joanna Szczurkowska; Francesca Pischedda; Bruno Pinto; Francesca Managò; Carola A Haas; Maria Summa; Rosalia Bertorelli; Francesco Papaleo; Michael K Schäfer; Giovanni Piccoli; Laura Cancedda
Journal:  Brain       Date:  2018-09-01       Impact factor: 13.501

3.  Apert Syndrome With FGFR2 758 C > G Mutation: A Chinese Case Report.

Authors:  Yahong Li; Dingyuan Ma; Yun Sun; Lulu Meng; Yanyun Wang; Tao Jiang
Journal:  Front Genet       Date:  2018-05-17       Impact factor: 4.599

4.  Language Impairments in ASD Resulting from a Failed Domestication of the Human Brain.

Authors:  Antonio Benítez-Burraco; Wanda Lattanzi; Elliot Murphy
Journal:  Front Neurosci       Date:  2016-08-29       Impact factor: 5.152
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.