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Services for Patients with Rare Genetic Diseases in Germany | Synapse
March 3, 2026
Open Access
Services for Patients with Rare Genetic Diseases in Germany
CS
Claudia Schmidtke
Humboldt-Universität zu Berlin
PK
Peter Kühnen
KM
Knut Mai
Humboldt-Universität zu Berlin
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Puntos clave
Improved patient access to healthcare services for rare genetic diseases is necessary in Germany.
Only a limited number of healthcare services effectively cater to the needs of patients with rare diseases.
Observational analysis examines the current status and implications of healthcare services for rare genetic diseases.
The findings highlight the need for enhanced support systems for patients with rare genetic diseases.
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Schmidtke et al. (Sat,) studied this question.
synapsesocial.com/papers/69a75f98c6e9836116a2b13d
https://doi.org/https://doi.org/10.1007/s12687-026-00865-z
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