Literature DB >> 16861145

Autism and Williams syndrome: a case report.

Sabri Herguner1, Nahit Motavalli Mukaddes.   

Abstract

Williams syndrome (WS) is a neurodevelopmental disorder caused by a deletion in the 7q11.23 region which includes at least 17 genes. The presence of autistic features in WS is a controversial issue. While some authors describe WS as the opposite phenotype of autism, recent studies indicate that both share many common characteristics. We report a 12-year-old boy diagnosed as autistic disorder and WS with hemizygosity at the elastin locus and a karyotype of 46,XY,del(7)(q11.21q11.23). Molecular genetic studies have shown that deletion at the elastin gene may account for the cardiovascular abnormalities seen in WS, but autistic features are likely caused by other genes flanking elastin.

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Year:  2006        PMID: 16861145     DOI: 10.1080/15622970600584221

Source DB:  PubMed          Journal:  World J Biol Psychiatry        ISSN: 1562-2975            Impact factor:   4.132


  11 in total

1.  Honing in on the social phenotype in Williams syndrome using multiple measures and multiple raters.

Authors:  Bonita P Klein-Tasman; Kirsten T Li-Barber; Erin T Magargee
Journal:  J Autism Dev Disord       Date:  2011-03

2.  Overlap with the autism spectrum in young children with Williams syndrome.

Authors:  Bonita P Klein-Tasman; Kristin D Phillips; Catherine Lord; Carolyn B Mervis; Frank J Gallo
Journal:  J Dev Behav Pediatr       Date:  2009-08       Impact factor: 2.225

Review 3.  Copy number variants at Williams-Beuren syndrome 7q11.23 region.

Authors:  Giuseppe Merla; Nicola Brunetti-Pierri; Lucia Micale; Carmela Fusco
Journal:  Hum Genet       Date:  2010-05-01       Impact factor: 4.132

4.  Autism, language delay and mental retardation in a patient with 7q11 duplication.

Authors:  C Depienne; D Heron; C Betancur; B Benyahia; O Trouillard; D Bouteiller; A Verloes; E Leguern; M Leboyer; A Brice
Journal:  BMJ Case Rep       Date:  2009-06-18

5.  Autism, language delay and mental retardation in a patient with 7q11 duplication.

Authors:  C Depienne; D Heron; C Betancur; B Benyahia; O Trouillard; D Bouteiller; A Verloes; E LeGuern; M Leboyer; A Brice
Journal:  J Med Genet       Date:  2007-03-30       Impact factor: 6.318

6.  Genetic testing in children with autism spectrum disorders.

Authors:  Esra Çöp; Pinar Yurtbaşi; Özgür Öner; Kerim M Münir
Journal:  Anadolu Psikiyatri Derg       Date:  2015       Impact factor: 0.518

7.  Autistic disorder in patients with Williams-Beuren syndrome: a reconsideration of the Williams-Beuren syndrome phenotype.

Authors:  Sylvie Tordjman; George M Anderson; Michel Botbol; Annick Toutain; Pierre Sarda; Michèle Carlier; Pascale Saugier-Veber; Clarisse Baumann; David Cohen; Céline Lagneaux; Anne-Claude Tabet; Alain Verloes
Journal:  PLoS One       Date:  2012-03-06       Impact factor: 3.240

8.  Genomic sister-disorders of neurodevelopment: an evolutionary approach.

Authors:  Bernard Crespi; Kyle Summers; Steve Dorus
Journal:  Evol Appl       Date:  2009-01-07       Impact factor: 5.183

9.  Atypical right diaphragmatic hernia (hernia of Morgagni), spigelian hernia and epigastric hernia in a patient with Williams syndrome: a case report.

Authors:  Farhan Rashid; Ramakrishna Chaparala; Javed Ahmed; Syed Y Iftikhar
Journal:  J Med Case Rep       Date:  2009-01-07

10.  Presence of autism, hyperserotonemia, and severe expressive language impairment in Williams-Beuren syndrome.

Authors:  Sylvie Tordjman; George M Anderson; David Cohen; Solenn Kermarrec; Michèle Carlier; Yvan Touitou; Pascale Saugier-Veber; Céline Lagneaux; Claire Chevreuil; Alain Verloes
Journal:  Mol Autism       Date:  2013-08-23       Impact factor: 7.509

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