Navigating Adulthood with Maple Syrup Urine Disease: Patient and Caregiver Perspectives on Healthcare Transition and Independent Living
Jessica I Gold, Megan Grabill, Karen Dolins, Meliss Basile, Bat-Zion Hose, Rebecca Ganetzky

TL;DR
People with Maple Syrup Urine Disease are living into adulthood and need better healthcare transition support for independent living.
Contribution
This study provides patient and caregiver insights into healthcare transition and adult life challenges for Maple Syrup Urine Disease.
Findings
Healthcare transition for MSUD is poor and non-standardized.
Adults with MSUD face new symptoms like fatigue and brain fog.
Functional outcomes vary widely in education, employment, and independence.
Abstract
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 typically diagnosed through population-level newborn screening, which allows for early treatment of dietary restrictions of branched chain amino acids and…
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Taxonomy
TopicsMetabolism and Genetic Disorders · Biochemical and Molecular Research · Genomics and Rare Diseases
