Navigating adulthood with maple syrup urine disease: patient and caregiver perspectives on healthcare transition and independent living

Abstract Background Medical advances in diagnosis and management have increased the life expectancy of many pediatric-onset rare diseases, including inherited metabolic disorders (IMDs). Historically fatal childhood conditions are now manageable chronic illnesses, with over 90% of individuals with IMD reaching adulthood. As more individuals with IMDs reach adulthood (age 18 years), there is a new imperative for health care transition planning that promotes developmentally-appropriate skills for medical self-management and independent living. Knowledge gaps on the long-term disease-related outcomes limit our ability to provide evidence-based resources for transition. Maple Syrup Urine Disease (MSUD) is an IMD with a global incidence of 1:185,000. It is increasingly diagnosed through population-level newborn screening, which allows for early treatment with dietary restrictions of branched chain amino acids and urgent intervention during episodes of catabolic stress. Due to the success of newborn screening programs, there is a growing population of adults with MSUD, making it a model for exploring the current state of transition and adult outcomes in IMDs. Results We used a qualitative case-study approach to assess the lived experiences of adults with MSUD ( n = 10) or caregivers to adults with MSUD ( n = 8). Analysis of their semi-structured interviews identified common themes including: (1) poor, non-standardized health care transition; (2) less emphasis on dietary management; (3) changing symptomatology with new presentations of fatigue, brain fog, and panic attacks; (3) emerging concerns related to adult health care, including comorbid adult-onset conditions, mental health, and lack of knowledgeable adult providers; (4) wide-ranging functional outcomes for education, employment, and financial independence; and (5) attainment of new milestones including romantic partnership and parenthood; and (6) greater concern about the supports needed to achieve independent living. Conclusions Individuals with MSUD are reaching milestones of adulthood and have new priorities for their healthcare and lifestyle. Evidence-based healthcare transition is needed to support their transition to independent living.

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Publication Details

Journal
Orphanet Journal of Rare Diseases
Published
2026-07-25
DOI
https://doi.org/10.1186/s13023-026-04383-6
Primary Topic
Metabolism and Genetic Disorders
Type
article
Field-Weighted Citation Impact
0.00

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article

Navigating adulthood with maple syrup urine disease: patient and caregiver perspectives on healthcare transition and independent living

Jessica I. Gold, Bat‐Zion Hose, Megan Grabill, Karen Dolins et al.
Orphanet Journal of Rare Diseases
Metabolism and Genetic Disorders
article

Navigating adulthood with maple syrup urine disease: patient and caregiver perspectives on healthcare transition and independent living

Jessica I. Gold, Bat‐Zion Hose, Megan Grabill, Karen Dolins, Melissa Basile, Rebecca Ganetzky
article en

Abstract

Abstract Background Medical advances in diagnosis and management have increased the life expectancy of many pediatric-onset rare diseases, including inherited metabolic disorders (IMDs). Historically fatal childhood conditions are now manageable chronic illnesses, with over 90% of individuals with IMD reaching adulthood. As more individuals with IMDs reach adulthood (age 18 years), there is a new imperative for health care transition planning that promotes developmentally-appropriate skills for medical self-management and independent living. Knowledge gaps on the long-term disease-related outcomes limit our ability to provide evidence-based resources for transition. Maple Syrup Urine Disease (MSUD) is an IMD with a global incidence of 1:185,000. It is increasingly diagnosed through population-level newborn screening, which allows for early treatment with dietary restrictions of branched chain amino acids and urgent intervention during episodes of catabolic stress. Due to the success of newborn screening programs, there is a growing population of adults with MSUD, making it a model for exploring the current state of transition and adult outcomes in IMDs. Results We used a qualitative case-study approach to assess the lived experiences of adults with MSUD ( n = 10) or caregivers to adults with MSUD ( n = 8). Analysis of their semi-structured interviews identified common themes including: (1) poor, non-standardized health care transition; (2) less emphasis on dietary management; (3) changing symptomatology with new presentations of fatigue, brain fog, and panic attacks; (3) emerging concerns related to adult health care, including comorbid adult-onset conditions, mental health, and lack of knowledgeable adult providers; (4) wide-ranging functional outcomes for education, employment, and financial independence; and (5) attainment of new milestones including romantic partnership and parenthood; and (6) greater concern about the supports needed to achieve independent living. Conclusions Individuals with MSUD are reaching milestones of adulthood and have new priorities for their healthcare and lifestyle. Evidence-based healthcare transition is needed to support their transition to independent living.

Orphanet Journal of Rare Diseases
Northwell Health (US), Feinstein Institute for Medical Research (US), Children's Hospital of Philadelphia (US), University of California, Los Angeles (US), Georgetown University (US), Maple Syrup Urine Disease Family Support Group (US), Cohen Children's Medical Center (US), Columbia University (US), University of Pennsylvania (US), MedStar Health (US)
National Institute of General Medical Sciences, Orphan Disease Center, Perelman School of Medicine, University of Pennsylvania
Openalex Percentile: Top 11%
Metabolism and Genetic Disorders
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