Search Results 1-10 of 17101 for Alkaptonuria
PKU is caused by a change in the gene that helps create an enzyme needed to break down phenylalanine. Treatment includes a special diet and medication.
Nitisinone is also used to reduce urine homogentisic acid (HGA) in patients with alkaptonuria (AKU), a rare inherited genetic disorder. This medicine is ...
Learn what to expect from this surgery that involves removing an adrenal gland.
Over time, the cysts may cause the kidneys to get bigger and stop working. PKD is most often passed through families. This is called an inherited condition.
The purpose of this study is to assess liver safety, non-liver safety, and effectiveness in subjects who previously experienced liver chemistry test ...
The primary objective of this study is to evaluate the effect of tolvaptan on the need for renal replacement therapy in pediatric subjects with autosomal ...
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