[article] 
inJournal of Autism and Developmental Disorders > 50-6 (June 2020) . - p.2174-2187

Titre :	Growing up with Fragile X Syndrome: Concerns and Care Needs of Young Adult Patients and Their Parents
Type de document :	Texte imprimé et/ou numérique
Auteurs :	M. C. VAN REMMERDEN, Auteur ; L. HOOGLAND, Auteur ; S. E. MOUS, Auteur ; Bram DIERCKX, Auteur ; M. COESMANS, Auteur ; H. A. MOLL, Auteur ; K. LUBBERS, Auteur ; C. R. LINCKEN, Auteur ; A. M. VAN EEGHEN, Auteur
Article en page(s) :	p.2174-2187
Langues :	Anglais (eng)
Mots-clés :	Fragile X syndrome (FXS)  ICF classification  Intellectual disability  Neurodevelopmental disorders  Qualitative research  Transition
Index. décimale :	PER Périodiques
Résumé :	Little is known about care needs of young adults with Fragile X Syndrome (FXS). Patient-driven information is needed to improve understanding and support of young adults with FXS. A qualitative study was performed in 5 young adult patients (aged 18-30), and 33 parents of young adults. Concerns and care needs were categorized using the International Classification of Functioning, Disability, and Health. Results indicated concerns on 14 domains for males, and 13 domains for females, including physical, psychological and socio-economical issues. In both groups parents reported high stress levels and a lack of knowledge of FXS in adult care providers. This study revealed concerns on various domains, requiring gender-specific, multidisciplinary transitional care and adult follow-up for patients with FXS.
En ligne :	http://dx.doi.org/10.1007/s10803-019-03973-7
Permalink :	https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=425

[article] Growing up with Fragile X Syndrome: Concerns and Care Needs of Young Adult Patients and Their Parents [Texte imprimé et/ou numérique] / M. C. VAN REMMERDEN, Auteur ; L. HOOGLAND, Auteur ; S. E. MOUS, Auteur ; Bram DIERCKX, Auteur ; M. COESMANS, Auteur ; H. A. MOLL, Auteur ; K. LUBBERS, Auteur ; C. R. LINCKEN, Auteur ; A. M. VAN EEGHEN, Auteur . - p.2174-2187.
Langues : Anglais (eng)
in Journal of Autism and Developmental Disorders > 50-6 (June 2020) . - p.2174-2187

Mots-clés :	Fragile X syndrome (FXS)  ICF classification  Intellectual disability  Neurodevelopmental disorders  Qualitative research  Transition
Index. décimale :	PER Périodiques
Résumé :	Little is known about care needs of young adults with Fragile X Syndrome (FXS). Patient-driven information is needed to improve understanding and support of young adults with FXS. A qualitative study was performed in 5 young adult patients (aged 18-30), and 33 parents of young adults. Concerns and care needs were categorized using the International Classification of Functioning, Disability, and Health. Results indicated concerns on 14 domains for males, and 13 domains for females, including physical, psychological and socio-economical issues. In both groups parents reported high stress levels and a lack of knowledge of FXS in adult care providers. This study revealed concerns on various domains, requiring gender-specific, multidisciplinary transitional care and adult follow-up for patients with FXS.
En ligne :	http://dx.doi.org/10.1007/s10803-019-03973-7
Permalink :	https://www.cra-rhone-alpes.org/cid/opac_css/index.php?lvl=notice_display&id=425