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Rare diseases in Croatia - No registry, no new therapies, no support

Author: Roberta Mlinarić

ZAGREB, 28 Feb (Hina) - Croatia lacks a rare disease patient registry, which limits access to therapies and medications, while social and psychological support remains insufficient, the national alliance representing rare disease patients said on the occasion of International Rare Disease Day, 28 February.

(Hina) rml

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