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A holistic approach to fragile X syndrome integrated guidance for person-centred care.
Johnson, Kirsten; Stanfield, Andrew C; Scerif, Gaia; McKechanie, Andrew; Clarke, Angus; Herring, Jonathan; Smith, Kayla; Crawford, Hayley.
Afiliação
  • Johnson K; The Fragile X Society, Great Dunmow, Essex, UK.
  • Stanfield AC; Fragile X International, Brussels, Belgium.
  • Scerif G; The Fragile X Society, Great Dunmow, Essex, UK.
  • McKechanie A; The Patrick Wild Centre, The University of Edinburgh, Edinburgh, UK.
  • Clarke A; Department of Experimental Psychology, University of Oxford, Oxford, UK.
  • Herring J; The Patrick Wild Centre, The University of Edinburgh, Edinburgh, UK.
  • Smith K; The Fragile X Society, Great Dunmow, Essex, UK.
  • Crawford H; Institute of Cancer & Genetics, Cardiff University, Cardiff, UK.
J Appl Res Intellect Disabil ; 37(3): e13214, 2024 May.
Article em En | MEDLINE | ID: mdl-38383947
ABSTRACT

BACKGROUND:

The Fragile X community has expressed a desire for centralised, national guidelines in the form of integrated guidance for Fragile X Syndrome (FXS).

METHODS:

This article draws on existing literature reviews, primary research and clinical trials on FXS, a Fragile X Society conference workshop and first-hand experience of clinicians who have worked with those living with FXS over many years.

RESULTS:

The article scopes proposed integrated guidance over the life course, including appendices of symptoms, comorbidities and referral options for FXS and Fragile X Premutation Associated Conditions.

CONCLUSION:

Integrated guidance would provide an authoritative source for doctors, health professionals, therapists, care workers, social workers, educators, employers, families and those living with FXS, so that a holistic, person-centred approach can be taken across the United Kingdom to garner the best outcomes for those with FXS.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome do Cromossomo X Frágil / Deficiência Intelectual Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome do Cromossomo X Frágil / Deficiência Intelectual Limite: Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article