Literature DB >> 9754629

Autistic symptoms among children and young adults with isodicentric chromosome 15.

S Rineer1, B Finucane, E W Simon.   

Abstract

A standardized assessment of autistic symptomatology was completed for 29 children and young adults with a supernumerary isodicentric chromosome 15 (formerly known as inverted duplication 15). Although there was variability in severity, 20 individuals with an isodicentric chromosome 15 [idic(15)] had a high probability of being autistic. Eight of the 9 remaining children were under age 5 years and were more sociable than the rest of the cohort. Group characteristics such as gender and seizure presence could not explain the observed difference between older and younger individuals in our study. The natural history of isodicentric 15 syndrome remains to be shown through longitudinal work and may include an age-related risk for developing autism.

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Year:  1998        PMID: 9754629     DOI: 10.1002/(sici)1096-8628(19980907)81:5<428::aid-ajmg12>3.0.co;2-e

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  24 in total

Review 1.  Specific genetic disorders and autism: clinical contribution towards their identification.

Authors:  David Cohen; Nadège Pichard; Sylvie Tordjman; Clarisse Baumann; Lydie Burglen; Elsa Excoffier; Gabriela Lazar; Philippe Mazet; Clément Pinquier; Alain Verloes; Delphine Héron
Journal:  J Autism Dev Disord       Date:  2005-02

2.  Characterization of an autism-associated segmental maternal heterodisomy of the chromosome 15q11-13 region.

Authors:  Dorota A Kwasnicka-Crawford; Wendy Roberts; Stephen W Scherer
Journal:  J Autism Dev Disord       Date:  2007-04

3.  Supernumerary marker chromosome 15 in a male with azoospermia and open bite deformity.

Authors:  Altuğ Koç; S Odül Onur; Mehmet Ali Ergün; E Ferda Perçin
Journal:  Asian J Androl       Date:  2009-08-24       Impact factor: 3.285

4.  A paternally inherited duplication in the Prader-Willi/Angelman syndrome critical region: a case and family study.

Authors:  Marijcke W M Veltman; Russell J Thompson; Ellen E Craig; Nicholas R Dennis; Sian E Roberts; Vanessa Moore; Josie A Brown; Patrick F Bolton
Journal:  J Autism Dev Disord       Date:  2005-02

5.  Autism spectrum disorders and symptoms in children with molecularly confirmed 22q11.2 deletion syndrome.

Authors:  Sarah E Fine; Alison Weissman; Marsha Gerdes; Jennifer Pinto-Martin; Elaine H Zackai; Donna M McDonald-McGinn; Beverly S Emanuel
Journal:  J Autism Dev Disord       Date:  2005-08

6.  Isodicentric Chromosome 15 Syndrome in a Korean Patient With Café-au-lait Spots.

Authors:  John Hoon Rim; Hee Jung Chung; Saeam Shin; Seo-Jin Park; Jong Rak Choi
Journal:  Ann Lab Med       Date:  2015-05-21       Impact factor: 3.464

Review 7.  Autism: in search of susceptibility genes.

Authors:  Janine A Lamb; Jeremy R Parr; Anthony J Bailey; Anthony P Monaco
Journal:  Neuromolecular Med       Date:  2002       Impact factor: 3.843

8.  Gabrb3 gene deficient mice exhibit impaired social and exploratory behaviors, deficits in non-selective attention and hypoplasia of cerebellar vermal lobules: a potential model of autism spectrum disorder.

Authors:  Timothy M DeLorey; Peyman Sahbaie; Ezzat Hashemi; Gregg E Homanics; J David Clark
Journal:  Behav Brain Res       Date:  2007-09-14       Impact factor: 3.332

9.  Eye movement abnormality suggestive of a spatial working memory deficit is present in parents of autistic probands.

Authors:  Dianne L Koczat; Sally J Rogers; Bruce F Pennington; Randal G Ross
Journal:  J Autism Dev Disord       Date:  2002-12

10.  Genomic and epigenetic evidence for oxytocin receptor deficiency in autism.

Authors:  Simon G Gregory; Jessica J Connelly; Aaron J Towers; Jessica Johnson; Dhani Biscocho; Christina A Markunas; Carla Lintas; Ruth K Abramson; Harry H Wright; Peter Ellis; Cordelia F Langford; Gordon Worley; G Robert Delong; Susan K Murphy; Michael L Cuccaro; Antonello Persico; Margaret A Pericak-Vance
Journal:  BMC Med       Date:  2009-10-22       Impact factor: 8.775

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