Nityr — Medica
Alkaptonuria
Initial criteria
- Diagnosis is supported by ONE of the following (i or ii): i) Genetic testing confirms biallelic pathogenic or likely pathogenic variants in the homogentisate 1,2 dioxygenase (HGD) gene; OR ii) Patient has elevated levels of homogentisic acid (HGA) in the urine
- Medication is prescribed by or in consultation with a rheumatologist or metabolic disease specialist (or specialist who focuses in the treatment of metabolic diseases)
Approval duration
1 year