↓ Skip to main content

JIMD Reports, Volume 33

Overview of attention for book
Cover of 'JIMD Reports, Volume 33'

Table of Contents

  1. Altmetric Badge
    Book Overview
  2. Altmetric Badge
    Chapter 528 Missed Newborn Screening Case of Carnitine Palmitoyltransferase-II Deficiency
  3. Altmetric Badge
    Chapter 535 Clinical and Genetic Characteristics of Romanian Patients with Mucopolysaccharidosis Type II
  4. Altmetric Badge
    Chapter 559 Leigh-Like Syndrome Due to Homoplasmic m.8993T>G Variant with Hypocitrullinemia and Unusual Biochemical Features Suggestive of Multiple Carboxylase Deficiency (MCD)
  5. Altmetric Badge
    Chapter 569 The Challenges of a Successful Pregnancy in a Patient with Adult Refsum’s Disease due to Phytanoyl-CoA Hydroxylase Deficiency
  6. Altmetric Badge
    Chapter 573 Difficulties in Daily Life and Associated Factors, and QoL of Children with Inherited Metabolic Disease and Their Parents in Japan: A Literature Review
  7. Altmetric Badge
    Chapter 575 Gastrointestinal Health in Classic Galactosemia
  8. Altmetric Badge
    Chapter 576 Swallow Prognosis and Follow-Up Protocol in Infantile Onset Pompe Disease
  9. Altmetric Badge
    Chapter 578 Management of Life-Threatening Tracheal Stenosis and Tracheomalacia in Patients with Mucopolysaccharidoses
  10. Altmetric Badge
    Chapter 579 Brain White Matter Integrity Mediates the Relationship Between Phenylalanine Control and Executive Abilities in Children with Phenylketonuria
  11. Altmetric Badge
    Chapter 580 Novel Homozygous Missense Mutation in SPG20 Gene Results in Troyer Syndrome Associated with Mitochondrial Cytochrome c Oxidase Deficiency
  12. Altmetric Badge
    Chapter 581 Lethal Neonatal LTBL Associated with Biallelic EARS2 Variants: Case Report and Review of the Reported Neuroradiological Features
  13. Altmetric Badge
    Chapter 582 Leukoencephalopathy due to Complex II Deficiency and Bi-Allelic SDHB Mutations: Further Cases and Implications for Genetic Counselling
  14. Altmetric Badge
    Chapter 583 Peak Jump Power Reflects the Degree of Ambulatory Ability in Patients with Mitochondrial and Other Rare Diseases
  15. Altmetric Badge
    Chapter 584 RARS2 Mutations: Is Pontocerebellar Hypoplasia Type 6 a Mitochondrial Encephalopathy?
  16. Altmetric Badge
    Chapter 587 Erratum: Missed Newborn Screening Case of Carnitine Palmitoyltransferase-II Deficiency
  17. Altmetric Badge
    Chapter 588 Erratum: Leigh-Like Syndrome Due to Homoplasmic m.8993T>G Variant with Hypocitrullinemia and Unusual Biochemical Features Suggestive of Multiple Carboxylase Deficiency (MCD).
Attention for Chapter 573: Difficulties in Daily Life and Associated Factors, and QoL of Children with Inherited Metabolic Disease and Their Parents in Japan: A Literature Review
Altmetric Badge

Readers on

mendeley
21 Mendeley
You are seeing a free-to-access but limited selection of the activity Altmetric has collected about this research output. Click here to find out more.
Chapter title
Difficulties in Daily Life and Associated Factors, and QoL of Children with Inherited Metabolic Disease and Their Parents in Japan: A Literature Review
Chapter number 573
Book title
JIMD Reports, Volume 33
Published in
JIMD Reports, January 2016
DOI 10.1007/8904_2016_573
Pubmed ID
Book ISBNs
978-3-66-255011-3, 978-3-66-255012-0
Authors

Keiko Yamaguchi, Rie Wakimizu, Mitsuru Kubota, Yamaguchi, Keiko, Wakimizu, Rie, Kubota, Mitsuru

Abstract

To assess the quality of life (QoL) of children in Japan with inborn errors of metabolism (IEM) as well as of their parents, we reviewed 23 previous studies published in Japanese and 1 published in English, focusing on the difficulties they encounter in daily life, the factors associated with these difficulties, and their QoL. We divided the difficulties and associated factors into three developmental stages. At the infant stage, individuals with IEM tend to be at high risk of hypercatabolism. Their parents suffered anxiety and distress because of the child's diet therapy and regarded the parents' support group as an essential presence, particularly given that IEM is a rare disease. At the school-age stage, as their sphere of social relationships expanded, children with IEM became nervous about being compared with healthy children of their own age because of their diet therapy. At the adolescence-to-adulthood stage, the children suffered medically, economically, and socially. Even in the absence of any IEM symptoms, the children's QoL was affected by the demands associated with the metabolic disorder, such as diet and treatment. The psychological health of their caregivers was also poor. To improve the QoL of children with IEM and of their parents, future comprehensive quantitative and qualitative studies of their QoL and of their subjective support needs are required. Additionally, the specific factors related to the QoL of such individuals need to be explored in large population-based statistical studies.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 21 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 21 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 4 19%
Student > Ph. D. Student 3 14%
Student > Postgraduate 2 10%
Student > Bachelor 2 10%
Student > Doctoral Student 1 5%
Other 2 10%
Unknown 7 33%
Readers by discipline Count As %
Nursing and Health Professions 4 19%
Psychology 4 19%
Immunology and Microbiology 1 5%
Pharmacology, Toxicology and Pharmaceutical Science 1 5%
Social Sciences 1 5%
Other 1 5%
Unknown 9 43%