More than 1,000 cases of alkaptonuria have been reported in the medical literature. Individuals from any group can potentially develop the disease, regardless of their sex, race or other factors.

Alkaptonuria is a rare genetic disorder that causes homogentisic acid to build up in your body. Learn about the symptoms, causes, and treatment.

The Egyptian mummy Harwa, dating from 1500 b.c., had alkaptonuria, 23 but the term “alcapton” was first used in 1859 to describe a patient's urinary reducing compound, 24 later identified as 2 ...

A new study published in The Lancet, led by a Liverpool based research collaboration, has identified the first effective treatment for a rare genetic condition known as alkaptonuria (AKU).

INDIANAPOLIS — Researchers from Indiana University School of Medicine diagnosed a Sumatran orangutan at the Indianapolis Zoo with a rare genetic disease. Mila, a 6-year-old orangutan who was ...

"New treatment for ultra-rare disease, alkaptonuria." ScienceDaily. www.sciencedaily.com / releases / 2018 / 08 / 180801102554.htm (accessed June 2, 2025). Explore More ...

Alkaptonuria is a rare genetic disorder caused by a deficiency of the enzyme homogentisate 1,2-dioxygenase. In an interview with HT Lifestyle, Dr Abhishek Agrawal, Consultant urologist, Jupiter ...

Nitisinone reduced HGA levels and improved symptoms in patients with alkaptonuria. The Food and Drug Administration (FDA) has approved Harliku ™ (nitisinone) for the reduction of urine ...

INDIANAPOLIS — Researchers from Indiana University School of Medicine diagnosed a Sumatran orangutan at the Indianapolis Zoo with a rare genetic disease. Mila, a 6-year-old orangutan who was born at ...