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Anupama Kapadia
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Ampleness of Nitisinone for the Administration of Alkaptonuria
Alkaptonuria, a rare metabolic disorder caused by a deficiency in homogentisate 1,2-dioxygenase, leads to the accumulation of homogentisic acid (HGA) and subsequent deposition of ochronotic pigment in connective tissues. The clinical manifestations of alkaptonuria include musculoskeletal issues, such as arthritis and spinal involvement, along with ... Read More»
: J Obes Metab 2024, 7:218
10.4172/jomb.1000218Abstract Peer-reviewed Full Article Peer-reviewed Article PDF Mobile Full Article
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