Care of patients with Phenylketonuria (PKU) in Germany – a claims data analysis from 2013 to 2023

Abstract Background Phenylketonuria (PKU) is a rare inherited metabolic disorder requiring lifelong management to prevent neurological, psychiatric, and physical complications. Although early detection through newborn screening has improved outcomes, real-world evidence on long-term care and healthc...

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Xehetasun bibliografikoak

Egile Nagusiak:	Axel Boehnke, Lisa-Marie Müller, Constantin Heidecke, Alexa Benson, Aljoscha S. Neubauer, Ania C. Muntau
Formatua:	Artigo
Hizkuntza:	Inglês
Argitaratua:	BMC 2026-07-01
Saila:	Orphanet Journal of Rare Diseases
Gaiak:	Phenylketonuria (PKU) Rare disease HCRU Real-world data Comorbidities Pharmacological treatment
Sarrera elektronikoa:	https://doi.org/10.1186/s13023-026-04467-3
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