Literature DB >> 9856568

Angelman syndrome: are the estimates too low?

R H Buckley1, N Dinno, P Weber.   

Abstract

More than 300 cases of Angelman Syndrome (AS) have been reported. AS is still considered a clinical diagnosis because only approximately 80% of those individuals who meet the clinical criteria will have a maternal deletion of chromosome 15q11-13. Of the reported cases of AS, very few are of adults with AS. We present our findings on 11 adults with AS identified in a long-term residential care facility for persons with severe developmental disabilities. The diagnosis of AS was not recognized at the time of their admission but was established as part of our evaluation. Thus, there may be an underestimate of the true incidence of AS especially in adults with severe developmental disabilities.

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Year:  1998        PMID: 9856568     DOI: 10.1002/(sici)1096-8628(19981204)80:4<385::aid-ajmg15>3.0.co;2-9

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


  17 in total

1.  "You have to sit and explain it all, and explain yourself." Mothers' experiences of support services for their offspring with a rare genetic intellectual disability syndrome.

Authors:  Gemma Maria Griffith; Richard P Hastings; Susie Nash; Michael Petalas; Chris Oliver; Patricia Howlin; Joanna Moss; Jane Petty; Penelope Tunnicliffe
Journal:  J Genet Couns       Date:  2011-01-04       Impact factor: 2.537

2.  A neurodevelopmental survey of Angelman syndrome with genotype-phenotype correlations.

Authors:  Jennifer K Gentile; Wen-Hann Tan; Lucia T Horowitz; Carlos A Bacino; Steven A Skinner; Rene Barbieri-Welge; Astrid Bauer-Carlin; Arthur L Beaudet; Terry Jo Bichell; Hye-Seung Lee; Trilochan Sahoo; Susan E Waisbren; Lynne M Bird; Sarika U Peters
Journal:  J Dev Behav Pediatr       Date:  2010-09       Impact factor: 2.225

3.  Social-emotional processing in nonverbal individuals with Angelman syndrome: evidence from brain responses to known and novel names.

Authors:  A P Key; D Jones
Journal:  J Intellect Disabil Res       Date:  2018-11-23

4.  Eye gaze and pupillary response in Angelman syndrome.

Authors:  Michael P Hong; Janna L Guilfoyle; Lindsey N Mooney; Logan K Wink; Ernest V Pedapati; Rebecca C Shaffer; John A Sweeney; Craig A Erickson
Journal:  Res Dev Disabil       Date:  2017-07-24

5.  Angelman syndrome: Mutations influence features in early childhood.

Authors:  Wen-Hann Tan; Carlos A Bacino; Steven A Skinner; Irina Anselm; Rene Barbieri-Welge; Astrid Bauer-Carlin; Arthur L Beaudet; Terry Jo Bichell; Jennifer K Gentile; Daniel G Glaze; Lucia T Horowitz; Sanjeev V Kothare; Hye-Seung Lee; Mark P Nespeca; Sarika U Peters; Trilochan Sahoo; Dean Sarco; Susan E Waisbren; Lynne M Bird
Journal:  Am J Med Genet A       Date:  2011-01       Impact factor: 2.802

6.  Asystole during outbursts of laughing in a child with Angelman syndrome.

Authors:  W Y Vanagt; C F Pulles-Heintzberger; K Vernooy; R N Cornelussen; T Delhaas
Journal:  Pediatr Cardiol       Date:  2005 Nov-Dec       Impact factor: 1.655

Review 7.  [Anesthesia and Angelman syndrome].

Authors:  W Witte; C Nobel; J Hilpert
Journal:  Anaesthesist       Date:  2011-03-16       Impact factor: 1.041

8.  Angelman syndrome in adulthood.

Authors:  Anna M Larson; Julianna E Shinnick; Elias A Shaaya; Elizabeth A Thiele; Ronald L Thibert
Journal:  Am J Med Genet A       Date:  2014-11-26       Impact factor: 2.802

Review 9.  Angelman syndrome: etiology, clinical features, diagnosis, and management of symptoms.

Authors:  Renzo Guerrini; Romeo Carrozzo; Roberta Rinaldi; Paolo Bonanni
Journal:  Paediatr Drugs       Date:  2003       Impact factor: 3.022

10.  The prevalence and phenomenology of repetitive behavior in genetic syndromes.

Authors:  Joanna Moss; Chris Oliver; Kate Arron; Cheryl Burbidge; Katy Berg
Journal:  J Autism Dev Disord       Date:  2008-11-27
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