Literature DB >> 22350623

Young adults with MSUD and their transition to adulthood: psychosocial issues.

Wendy Packman1, Indira Mehta, Samantha Rafie, Jayanthi Mehta, Mariana Naldi, Kim Hart Mooney.   

Abstract

Maple Syrup Urine Disease (MSUD) is an autosomal recessive condition with an incidence of 1 in 185,000 births worldwide. Regardless of the type of MSUD, treatment includes immediate and lifelong dietary restriction of isoleucine, leucine and valine. There is little known about the psychosocial impact of MSUD on the developmental milestones of emerging adulthood. We used a qualitative case study approach to explore the human experiences of MSUD on young adults (n = 8) and parents (n = 8). All participants were administered a semi-structured, qualitative interview as well as quantitative measures. Six core themes emerged: 1) lifelong strain of dietary management; 2) social isolation from peers and impact on dating; 3) impact of MSUD on academics and employment; 4) medical experiences and transition to adult care; 5) impact on family functioning; and 6) positive effects and growth. The results of this investigation highlight and expand awareness of the psychological and social needs of young adults with MSUD. This study calls for a collaborative, multidisciplinary effort in the treatment of these patients and their families.

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Year:  2012        PMID: 22350623     DOI: 10.1007/s10897-012-9490-1

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


  25 in total

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6.  Adolescents' perspectives of chronic illness: "it's hard".

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Journal:  J Pediatr Nurs       Date:  1998-08       Impact factor: 2.145

7.  Transition of young adults with phenylketonuria from pediatric to adult care.

Authors:  Ulrike Mütze; Annika Roth; Johannes F W Weigel; Skadi Beblo; Christoph G Baerwald; Peter Bührdel; Wieland Kiess
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8.  Psychosocial functioning in youth with glycogen storage disease type I.

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9.  Parenting adolescent girls with type 1 diabetes: parents' perspectives.

Authors:  Alison E Mellin; Dianne Neumark-Sztainer; Joan M Patterson
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10.  Psychosocial aspects of patients with Niemann-Pick disease, type B.

Authors:  Shelly L Henderson; Wendy Packman; Seymour Packman
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  13 in total

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Authors:  Aaron S Kesselheim; Sarah McGraw; Lauren Thompson; Kelly O'Keefe; Joshua J Gagne
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2.  Living with Intoxication-Type Inborn Errors of Metabolism: A Qualitative Analysis of Interviews with Paediatric Patients and Their Parents.

Authors:  Nina A Zeltner; Markus A Landolt; Matthias R Baumgartner; Sarah Lageder; Julia Quitmann; Rachel Sommer; Daniela Karall; Chris Mühlhausen; Andrea Schlune; Sabine Scholl-Bürgi; Martina Huemer
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Authors:  Nina A Zeltner; Matthias R Baumgartner; Aljona Bondarenko; Regina Ensenauer; Daniela Karall; Stefan Kölker; Chris Mühlhausen; Sabine Scholl-Bürgi; Eva Thimm; Julia Quitmann; Peter Burgard; Markus A Landolt; Martina Huemer
Journal:  JIMD Rep       Date:  2017-03-01

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Authors:  Isabela da Silva Lemos; Leticia Burato Wessler; Mariane Bernardo Duarte; Guilherme Lodetti da Silva; Henrique Teza Bernardo; Gabriela Candiotto; Carolina Antunes Torres; Fabricia Petronilho; Eduardo Pacheco Rico; Emilio Luiz Streck
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5.  Exploring the Barriers and Motivators to Dietary Adherence among Caregivers of Children with Disorders of Amino Acid Metabolism (AAMDs): A Qualitative Study.

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Review 6.  The neuropsychiatry of inborn errors of metabolism.

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7.  Parent Coping and the Behavioural and Social Outcomes of Children Diagnosed with Inherited Metabolic Disorders.

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8.  Assessment of quality of life of the children and parents affected by inborn errors of metabolism with restricted diet: preliminary results of a cross-sectional study.

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9.  Brain-blood amino acid correlates following protein restriction in murine maple syrup urine disease.

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Review 10.  Branched-chain amino acid metabolism: from rare Mendelian diseases to more common disorders.

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Journal:  Hum Mol Genet       Date:  2014-03-20       Impact factor: 6.150

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