Movement Disorders and Syndromic Autism: A Systematic Review / L. BELL in Journal of Autism and Developmental Disorders, 49-1 (January 2019)  

Public ISBD [article]  inJournal of Autism and Developmental Disorders > 49-1 (January 2019) . - p.54-67 Titre : Movement Disorders and Syndromic Autism: A Systematic Review Type de document : Texte imprimé et/ou numérique Auteurs : L. BELL, Auteur ; A. WITTKOWSKI, Auteur ; D. J. HARE, Auteur Article en page(s) : p.54-67 Langues : Anglais (eng) Mots-clés : Angelman  Ataxia  Autism  Dystonia  Extra-pyramidal  Movement disorder  Retts  Rigidity  Tremor Index. décimale : PER Périodiques Résumé : Movement disorders are reported in idiopathic autism but the extent to which comparable movement disorders are found in syndromic/co-morbid autism is unknown. A systematic search of Medline, Embase, PsychINFO and CINAHL on the prevalence of specific movement disorder in syndromic autism associated with specific genetic syndromes identified 16 papers, all relating to Angelman syndrome or Rett syndrome. Prevalence rates of 72.7-100% and 25.0-27.3% were reported for ataxia and tremor, respectively, in Angelman syndrome. In Rett syndrome, prevalence rates of 43.6-50% were reported for ataxia and 27.3-48.3% for tremor with additional reports of dystonia, rigidity and pyramidal signs. However, reliable assessment measures were rarely used and recruitment was often not described in sufficient detail. En ligne : http://dx.doi.org/10.1007/s10803-018-3658-y Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=376 [article] Movement Disorders and Syndromic Autism: A Systematic Review [Texte imprimé et/ou numérique] / L. BELL, Auteur ; A. WITTKOWSKI, Auteur ; D. J. HARE, Auteur . - p.54-67. Langues : Anglais (eng) in Journal of Autism and Developmental Disorders > 49-1 (January 2019) . - p.54-67 Mots-clés : Angelman  Ataxia  Autism  Dystonia  Extra-pyramidal  Movement disorder  Retts  Rigidity  Tremor Index. décimale : PER Périodiques Résumé : Movement disorders are reported in idiopathic autism but the extent to which comparable movement disorders are found in syndromic/co-morbid autism is unknown. A systematic search of Medline, Embase, PsychINFO and CINAHL on the prevalence of specific movement disorder in syndromic autism associated with specific genetic syndromes identified 16 papers, all relating to Angelman syndrome or Rett syndrome. Prevalence rates of 72.7-100% and 25.0-27.3% were reported for ataxia and tremor, respectively, in Angelman syndrome. In Rett syndrome, prevalence rates of 43.6-50% were reported for ataxia and 27.3-48.3% for tremor with additional reports of dystonia, rigidity and pyramidal signs. However, reliable assessment measures were rarely used and recruitment was often not described in sufficient detail. En ligne : http://dx.doi.org/10.1007/s10803-018-3658-y Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=376

Symptoms of Autism Spectrum Disorder (ASD) in Individuals with Mucopolysaccharide Disease Type III (Sanfilippo Syndrome): A Systematic Review / C. WOLFENDEN in Journal of Autism and Developmental Disorders, 47-11 (November 2017)  

Public ISBD [article]  inJournal of Autism and Developmental Disorders > 47-11 (November 2017) . - p.3620-3633 Titre : Symptoms of Autism Spectrum Disorder (ASD) in Individuals with Mucopolysaccharide Disease Type III (Sanfilippo Syndrome): A Systematic Review Type de document : Texte imprimé et/ou numérique Auteurs : C. WOLFENDEN, Auteur ; A. WITTKOWSKI, Auteur ; D. J. HARE, Auteur Article en page(s) : p.3620-3633 Langues : Anglais (eng) Mots-clés : Asd  Behavioural difficulties  Developmental disorder  Lysosomal storage disorder  Mucopolysacchardosis  Speech/language delay Index. décimale : PER Périodiques Résumé : The prevalence of autism spectrum disorder (ASD) in many genetic disorders is well documented but not as yet in Mucopolysaccharidosis type III (MPS III). MPS III is a recessively inherited metabolic disorder and evidence suggests that symptoms of ASD present in MPS III. This systematic review examined the extant literature on the symptoms of ASD in MPS III and quality assessed a total of 16 studies. Results indicated that difficulties within speech, language and communication consistent with ASD were present in MPS III, whilst repetitive and restricted behaviours and interests were less widely reported. The presence of ASD-like symptoms can result in late diagnosis or misdiagnosis of MPS III and prevent opportunities for genetic counselling and the provision of treatments. En ligne : http://dx.doi.org/10.1007/s10803-017-3262-6 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=325 [article] Symptoms of Autism Spectrum Disorder (ASD) in Individuals with Mucopolysaccharide Disease Type III (Sanfilippo Syndrome): A Systematic Review [Texte imprimé et/ou numérique] / C. WOLFENDEN, Auteur ; A. WITTKOWSKI, Auteur ; D. J. HARE, Auteur . - p.3620-3633. Langues : Anglais (eng) in Journal of Autism and Developmental Disorders > 47-11 (November 2017) . - p.3620-3633 Mots-clés : Asd  Behavioural difficulties  Developmental disorder  Lysosomal storage disorder  Mucopolysacchardosis  Speech/language delay Index. décimale : PER Périodiques Résumé : The prevalence of autism spectrum disorder (ASD) in many genetic disorders is well documented but not as yet in Mucopolysaccharidosis type III (MPS III). MPS III is a recessively inherited metabolic disorder and evidence suggests that symptoms of ASD present in MPS III. This systematic review examined the extant literature on the symptoms of ASD in MPS III and quality assessed a total of 16 studies. Results indicated that difficulties within speech, language and communication consistent with ASD were present in MPS III, whilst repetitive and restricted behaviours and interests were less widely reported. The presence of ASD-like symptoms can result in late diagnosis or misdiagnosis of MPS III and prevent opportunities for genetic counselling and the provision of treatments. En ligne : http://dx.doi.org/10.1007/s10803-017-3262-6 Permalink : https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=325

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