Nutritional interventions for patients with alkaptonuria: A minireview

Nutritional interventions for patients with alkaptonuria: A minireview

Alkaptonuria (AKU, OMIM, No. 203500) is a rare, slow-progressing, irreversible, multisystemic disease resulting from a deficiency of the homogentisate 1,2-dioxygenase enzyme, which leads to the accumulation of homogentisic acid (HGA) and subsequent deposition as pigment in connective tissues called...

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Bibliographic Details
Main Authors: Imrich Richard, Zatkova Andrea, Lukacova Olga, Sedlakova Jana, Zanova Elizabeth, Vlcek Miroslav, Penesova Adela, Radikova Zofia, Havranova Andrea, Ranganath Lakshminarayan
Format: Article
Language:English
Published: Sciendo 2023-01-01
Series:Endocrine Regulations
Subjects:
alkaptonuria
nitisinone
nutritional intervention
Online Access:https://doi.org/10.2478/enr-2023-0008

Internet

https://doi.org/10.2478/enr-2023-0008

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