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Suffers of the serious genetic condition phenylketonuria (PKU) are unable to convert phenylalanine to tyrosine, whilst patients with alkaptonuria have a defective tyrosine metabolism, producing distinctive urine which darkens when exposed to the air

The standard starting dose is 0.2 mg per night, injected subcutaneously

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Real world data on the epidemiology, diagnosis, and treatment of acromegaly: a registries-based approach