Literature DB >> 34292487

The Cost of Raising Individuals with Fragile X or Chromosome 15 Imprinting Disorders in Australia.

Emma K Baker1,2,3, Sheena Arora4, David J Amor2,5, Perrin Date1,6, Meagan Cross7, James O'Brien8, Chloe Simons7, Carolyn Rogers9, Stephen Goodall4, Jennie Slee10, Chris Cahir11, David E Godler12,13.   

Abstract

The study characterised differences in costs associated with raising a child between four rare disorders and examined the associations between these costs with clinical severity. Caregivers of 108 individuals with Prader-Willi, Angelman (AS), Chromosome 15q Duplication and fragile X (FXS) syndromes completed a modified Client Services Receipt Inventory and participants completed intellectual/developmental functioning and autism assessments. AS incurred the highest yearly costs per individual ($AUD96,994), while FXS had the lowest costs ($AUD33,221). Intellectual functioning negatively predicted total costs, after controlling for diagnosis. The effect of intellectual functioning on total costs for those with AS was significantly different to the other syndromes. The study highlights the significant costs associated with these syndromes, particularly AS, linked with severity of intellectual functioning.
© 2021. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  Angelman syndrome; Chromosome 15 Duplication syndrome; Fragile X syndrome; Health Economics; Prader-Willi syndrome

Year:  2021        PMID: 34292487     DOI: 10.1007/s10803-021-05193-4

Source DB:  PubMed          Journal:  J Autism Dev Disord        ISSN: 0162-3257


  24 in total

1.  A survey of seizures and current treatments in 15q duplication syndrome.

Authors:  Kerry D Conant; Brenda Finucane; Nicole Cleary; Ashley Martin; Candace Muss; Mary Delany; Erin K Murphy; Olivia Rabe; Kadi Luchsinger; Sarah J Spence; Carolyn Schanen; Orrin Devinsky; Edwin H Cook; Janine LaSalle; Lawrence T Reiter; Ronald L Thibert
Journal:  Epilepsia       Date:  2014-02-06       Impact factor: 5.864

2.  Societal cost of childhood intellectual disability in Australia.

Authors:  S Arora; S Goodall; R Viney; S Einfeld
Journal:  J Intellect Disabil Res       Date:  2020-04-24

3.  Endocrine disorders in children with Prader-Willi syndrome--data from 142 children of the French database.

Authors:  G Diene; E Mimoun; E Feigerlova; S Caula; C Molinas; H Grandjean; M Tauber
Journal:  Horm Res Paediatr       Date:  2010-04-15       Impact factor: 2.852

4.  The Italian National Survey for Prader-Willi syndrome: an epidemiologic study.

Authors:  Graziano Grugni; Antonino Crinò; Laura Bosio; Andrea Corrias; Marina Cuttini; Teresa De Toni; Eliana Di Battista; Adriana Franzese; Luigi Gargantini; Nella Greggio; Lorenzo Iughetti; Chiara Livieri; Arturo Naselli; Claudio Pagano; Giovanni Pozzan; Letizia Ragusa; Alessandro Salvatoni; Giuliana Trifirò; Luciano Beccaria; Maria Bellizzi; Jaele Bellone; Amelia Brunani; Marco Cappa; Gabriella Caselli; Valeria Cerioni; Maurizio Delvecchio; Daniela Giardino; Francesco Iannì; Luigi Memo; Alba Pilotta; Cristoforo Pomara; Giorgio Radetti; Michele Sacco; Annarosa Sanzari; Alessandro Sartorio; Giorgio Tonini; Roberto Vettor; Federico Zaglia; Giuseppe Chiumello
Journal:  Am J Med Genet A       Date:  2008-04-01       Impact factor: 2.802

5.  The aberrant behavior checklist: a behavior rating scale for the assessment of treatment effects.

Authors:  M G Aman; N N Singh; A W Stewart; C J Field
Journal:  Am J Ment Defic       Date:  1985-03

6.  Behavioral characterization of dup15q syndrome: Toward meaningful endpoints for clinical trials.

Authors:  Charlotte DiStefano; Rujuta B Wilson; Carly Hyde; Edwin H Cook; Ronald L Thibert; Lawrence T Reiter; Vanessa Vogel-Farley; Joerg Hipp; Shafali Jeste
Journal:  Am J Med Genet A       Date:  2019-10-26       Impact factor: 2.802

7.  Causes of death in Prader-Willi syndrome: Prader-Willi Syndrome Association (USA) 40-year mortality survey.

Authors:  Merlin G Butler; Ann M Manzardo; Janalee Heinemann; Carolyn Loker; James Loker
Journal:  Genet Med       Date:  2016-11-17       Impact factor: 8.822

8.  An overview of health issues and development in a large clinical cohort of children with Angelman syndrome.

Authors:  Karen G C B Bindels-de Heus; Sabine E Mous; Maartje Ten Hooven-Radstaake; Bianca M van Iperen-Kolk; Cindy Navis; André B Rietman; Leontine W Ten Hoopen; Alice S Brooks; Ype Elgersma; Henriëtte A Moll; Marie-Claire Y de Wit
Journal:  Am J Med Genet A       Date:  2019-11-15       Impact factor: 2.802

9.  Intragenic DNA methylation in buccal epithelial cells and intellectual functioning in a paediatric cohort of males with fragile X.

Authors:  Marta Arpone; Emma K Baker; Lesley Bretherton; Minh Bui; Xin Li; Simon Whitaker; Cheryl Dissanayake; Jonathan Cohen; Chriselle Hickerton; Carolyn Rogers; Mike Field; Justine Elliott; Solange M Aliaga; Ling Ling; David Francis; Stephen J C Hearps; Matthew F Hunter; David J Amor; David E Godler
Journal:  Sci Rep       Date:  2018-02-26       Impact factor: 4.379

10.  Exploring autism symptoms in an Australian cohort of patients with Prader-Willi and Angelman syndromes.

Authors:  Emma K Baker; David E Godler; Minh Bui; Chriselle Hickerton; Carolyn Rogers; Mike Field; David J Amor; Lesley Bretherton
Journal:  J Neurodev Disord       Date:  2018-08-06       Impact factor: 4.025

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