J Genet Med.  2024 Jun;21(1):1-5. 10.5734/JGM.2024.21.1.1.

Understanding and managing patients with adult rare diseases

Affiliations
  • 1Department of Genomic Medicine, Rare Disease Center, Seoul National University Hospital, Seoul, Korea
  • 2Department of Neurology, Rare Disease Center, Seoul National University Hospital, Seoul, Korea

Abstract

Despite advances in the diagnosis and management of rare diseases (RDs), there remains a tendency to overlook adult RD patients. In addition to the considerable number of adult-onset RDs, advances in the diagnosis and management of pediatric RDs have led to an increase in the survival of these patients into adulthood. Adult RDs exhibit distinct features from pediatric counterparts, necessitating careful consideration during medical assessments. Given the extended life expectancy of adult RD patients, precise diagnosis and management strategies can significantly enhance patient outcomes. This review aims to provide an in-depth exploration of the characteristics unique to adult RDs. Special emphasis will be placed on the importance of cascade screening and prenatal genetic testing in the context of adult RDs, highlighting the need for a comprehensive understanding of these aspects in clinical practice.

Keyword

Rare diseases; Late onset disorders; Genetic diseases; inborn; Genetic carrier screening; Genetic counseling
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