Literature DB >> 25597928

The Impact on the Family of Four Neurogenetic Syndromes: A Comparative Study of Parental Views.

Colin Reilly1, Lelia Murtagh2, Joyce Senior2.   

Abstract

Research on behavioral phenotypes in neurogenetic syndromes has primarily focused on aspects of the affected child's behavior. However, the impact of having a child with a neurogenetic syndrome on aspects of family functioning can be significant and differ across syndromes. Parents (N = 381) of school-aged children with one of four neurogenetic syndromes: fragile X Syndrome (FXS), Prader Willi Syndrome (PWS), Williams Syndrome (WS) and 22q11.2 (22qDEL) were asked about challenges, restrictions, future concerns and positive aspects arising from having an affected child. Factors associated with these aspects were analysed via logistic regression. Restrictions were most often reported by parents of children with FXS. The factors significantly (p < .01) associated with the parent reported restrictions were the presence of a behavioral/psychiatric condition and a lower level of receptive communication. The challenges endorsed most often were the child's learning and social skills difficulties. Significant differences (p < .01) between the syndromes were noted for many of the challenges. Ninety-six percent of parents endorsed at least one positive aspect but most aspects endorsed did not differ between the genetic syndromes. Having a behavioral/psychiatric condition was the only factor significantly associated (p < .01) with endorsing a lower number of positive aspects and a higher number of challenges. There are some commonalities but also significant differences across syndromes regarding views on how a child's syndrome affects family functioning. These differences may be important with regard to how to counsel and support affected families. The presence of behavioral/psychiatric conditions is an important predictor of negative family outcome across the syndromes.

Entities:  

Keywords:  Challenges; Impact; Neurogenetic; Positive

Mesh:

Year:  2015        PMID: 25597928     DOI: 10.1007/s10897-015-9820-1

Source DB:  PubMed          Journal:  J Genet Couns        ISSN: 1059-7700            Impact factor:   2.537


  29 in total

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2.  Positive psychology progress: empirical validation of interventions.

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3.  The impact of Prader-Willi syndrome on the family's quality of life and caregiving, and the unaffected siblings' psychosocial adjustment.

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Authors:  K Scorgie; D Sobsey
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5.  Neuropathology of fragile X-associated tremor/ataxia syndrome (FXTAS).

Authors:  C M Greco; R F Berman; R M Martin; F Tassone; P H Schwartz; A Chang; B D Trapp; C Iwahashi; J Brunberg; J Grigsby; D Hessl; E J Becker; J Papazian; M A Leehey; R J Hagerman; P J Hagerman
Journal:  Brain       Date:  2005-12-05       Impact factor: 13.501

6.  Positive contributions made by children with an intellectual disability in the family: mothers' and fathers' perceptions.

Authors:  Richard P Hastings; Alexandra Beck; Christopher Hill
Journal:  J Intellect Disabil       Date:  2005-06

7.  Positive perceptions in families of children with developmental disabilities.

Authors:  Richard P Hastings; Helen M Taunt
Journal:  Am J Ment Retard       Date:  2002-03

8.  Caregiver Burden in Fragile X Families.

Authors:  Ana-Maria Iosif; Andres F Sciolla; Khyati Brahmbhatt; Andreea L Seritan
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9.  Prevalence estimation of Williams syndrome.

Authors:  Petter Strømme; Per G Bjørnstad; Kjersti Ramstad
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10.  Longitudinal perspectives of child positive impact on families: relationship to disability and culture.

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  8 in total

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Authors:  Olympia Palikara; Maria Ashworth; Jo Van Herwegen
Journal:  J Autism Dev Disord       Date:  2018-09

2.  Brief Report: Challenging Behaviors in Toddlers and Preschoolers with Angelman, Prader-Willi, and Williams Syndromes.

Authors:  Wei Siong Neo; Bridgette L Tonnsen
Journal:  J Autism Dev Disord       Date:  2019-04

3.  Medical, welfare, and educational challenges and psychological distress in parents caring for an individual with 22q11.2 deletion syndrome: A cross-sectional survey in Japan.

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Journal:  Am J Med Genet A       Date:  2021-09-03       Impact factor: 2.578

Review 4.  Variables related to the quality of life of families that have a child with severe to profound intellectual disabilities: A systematic review.

Authors:  N Luitwieler; J Luijkx; M Salavati; C P Van der Schans; A J Van der Putten; A Waninge
Journal:  Heliyon       Date:  2021-06-24

5.  Life Satisfaction Among Mothers of Individuals with Prader-Willi Syndrome.

Authors:  Carolyn M Shivers; Caroline L Leonczyk; Elisabeth M Dykens
Journal:  J Autism Dev Disord       Date:  2016-06

6.  Parental stress and adjustment in the context of rare genetic syndromes: A scoping review.

Authors:  Jacqueline Fitzgerald; Louise Gallagher
Journal:  J Intellect Disabil       Date:  2021-04-19

7.  The psychosocial impact of 22q11 deletion syndrome on patients and families: A systematic review.

Authors:  Oanh Kieu Vo; Alisdair McNeill; Katharina Sophie Vogt
Journal:  Am J Med Genet A       Date:  2018-03-25       Impact factor: 2.802

Review 8.  Williams syndrome.

Authors:  Beth A Kozel; Boaz Barak; Chong Ae Kim; Carolyn B Mervis; Lucy R Osborne; Melanie Porter; Barbara R Pober
Journal:  Nat Rev Dis Primers       Date:  2021-06-17       Impact factor: 65.038

  8 in total

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