Ontology highlight
ABSTRACT:
SUBMITTER: Wolffenbuttel BHR
PROVIDER: S-EPMC8336241 | biostudies-literature | 2021 Aug
REPOSITORIES: biostudies-literature
Wolffenbuttel Bruce H R BHR Heiner-Fokkema M Rebecca MR van Spronsen Francjan J FJ
Orphanet journal of rare diseases 20210803 1
Alkaptonuria (AKU, OMIM 203500) is a rare congenital disorder caused by a deficiency of the enzyme homogentisate-1,2,-dioxygenase. The long-term consequences of AKU are joint problems, cardiac valve abnormalities and renal problems. Landmark intervention studies with nitisinone 10 mg daily, suppressing an upstream enzyme activity, demonstrated its beneficial effects in AKU patients with established complications, which usually start to develop in the fourth decade. Lower dose of nitisinone in th ...[more]