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Parental perspectives on Phelan-McDermid syndrome: Results of a worldwide survey.
Landlust, Annemiek M; Koza, Sylvia A; Carbin, Maya; Walinga, Margreet; Robert, Sandra; Cooke, Jennifer; Vyshka, Klea; van Balkom, Ingrid D C; van Ravenswaaij-Arts, Conny.
Afiliación
  • Landlust AM; Autism Team Northern-Netherlands, Jonx, Department of (Youth) Mental Health and Autism, Lentis Psychiatric Institute, Groningen, the Netherlands; University of Groningen, University Medical Centre Groningen, Department of Genetics, Groningen, the Netherlands. Electronic address: a.landlust@lentis.nl
  • Koza SA; University of Groningen, University Medical Centre Groningen, Department of Genetics, Groningen, the Netherlands.
  • Carbin M; Phelan-McDermid Association, the Netherlands.
  • Walinga M; University of Groningen, University Medical Centre Groningen, Department of Genetics, Groningen, the Netherlands.
  • Robert S; (Swiss Representative of) Phelan-McDermid-Gesellschaft e.V. Geschäftsstelle Universitätsklinikum Ulm, Sekretariat Neurologie, Ulm, Germany.
  • Cooke J; Forensic and Neurodevelopmental Sciences Department, Institute of Psychiatry, Psychology, and Neuroscience, King's College London, United Kingdom.
  • Vyshka K; ERN ITHACA Guideline Working Group, ERN ITHACA Project Management & Legal Office, Clinical Genetics Department, Robert Debré University Hospital, Paris, France.
  • van Balkom IDC; Autism Team Northern-Netherlands, Jonx, Department of (Youth) Mental Health and Autism, Lentis Psychiatric Institute, Groningen, the Netherlands; Rob Giel Research Centre, Department of Psychiatry, University Medical Center Groningen, Groningen, the Netherlands.
  • van Ravenswaaij-Arts C; Autism Team Northern-Netherlands, Jonx, Department of (Youth) Mental Health and Autism, Lentis Psychiatric Institute, Groningen, the Netherlands; University of Groningen, University Medical Centre Groningen, Department of Genetics, Groningen, the Netherlands.
Eur J Med Genet ; 66(7): 104771, 2023 Jul.
Article en En | MEDLINE | ID: mdl-37120079
ABSTRACT
Phelan-McDermid syndrome (PMS) is a rare neurodevelopmental disorder characterised by hypotonia, speech problems, intellectual disability and mental health issues like regression, autism and mood disorders. In the development, implementation and dissemination of a new clinical guideline for a rare genetic disorder like PMS, the parental experienced perspective is essential. As information from literature is scarce and often conflicting the European Phelan-McDermid syndrome guideline consortium created a multi-lingual survey for parents of individuals with PMS to collect their lived experiences with care needs, genotypes, somatic issues, mental health issues and parental stress. In total, we analysed 587 completed surveys from 35 countries worldwide. Based on parental reporting, PMS appeared to be caused by a deletion of chromosome 22q13.3 in 78% (379/486) of individuals and by a variant in the SHANK3 gene in 22% (107/486) of the individuals. Parents reported a wide variety of developmental, neurological, and other clinical issues in individuals with PMS. The most frequently experienced issues were related to speech and communication, learning disabilities/intellectual disability, and behaviour. While most reported issues were present across all age groups and genotypes, the prevalence of epilepsy, lymphoedema, and mental health issues do appear to vary with age. Developmental regression also appeared to begin earlier in this cohort than described in literature. Individuals with PMS due to a 22q13.3 deletion had a higher rate of kidney issues and lymphoedema compared to individuals with SHANK3 variants. Parental stress was high, with specific contributing factors being child and context related in accordance with the PMS phenotype. The survey results led to various validated recommendations in the European PMS guideline including an age specific surveillance scheme, specific genetic counselling, structured healthcare evaluations on sleep and communication and a focus on family well-being.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Trastornos de los Cromosomas / Discapacidad Intelectual Tipo de estudio: Guideline / Qualitative_research / Risk_factors_studies Límite: Humans Idioma: En Revista: Eur J Med Genet Asunto de la revista: GENETICA MEDICA Año: 2023 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Trastornos de los Cromosomas / Discapacidad Intelectual Tipo de estudio: Guideline / Qualitative_research / Risk_factors_studies Límite: Humans Idioma: En Revista: Eur J Med Genet Asunto de la revista: GENETICA MEDICA Año: 2023 Tipo del documento: Article