Abstract
From Sir Archibald Garrod's initial description of the tetrad of albinism, alkaptonuria, cystinuria, and pentosuria to today, the field of medicine dedicated to inborn errors of metabolism has evolved from disease identification and mechanistic discovery to the development of therapies designed to subvert biochemical defects. In this review, we highlight major milestones in the treatment and diagnosis of inborn errors of metabolism, starting with dietary therapy for phenylketonuria in the 1950s and 1960s, and ending with current approaches in genetic manipulation.
Author supplied keywords
Cite
CITATION STYLE
Vernon, H. J., & Manoli, I. (2021). Milestones in treatments for inborn errors of metabolism: Reflections on Where chemistry and medicine meet. American Journal of Medical Genetics, Part A, 185(11), 3350–3358. https://doi.org/10.1002/ajmg.a.62385
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.