Prader-Willijev sindrom (PWS)

Prader-Willijev sindrom (PWS) genetsko je stanje koje utječe na mnoge dijelove tijela. Dojenčad s PWS-om pati od teške hipotonije (nizak tonus mišića), poteškoća s hranjenjem i usporenog rasta. U kasnijoj dojenačkoj dobi ili ranom djetinjstvu oboljela djeca obično počinju pretjerano jesti i postaju gojazna.

The Croatian Alliance for Rare Diseases is a recipient of institutional support from the National Foundation for Civil Society Development for the stabilization and/or development of the association.
The content of the website is the sole responsibility of the Croatian Alliance for Rare Diseases
The creation of the website was co-financed by the European Union from the European Social Fund
European Union

Together for EU Funds

About us

Copyright 2020 Hrvatski savez za rijetke bolesti.
Development by Fugaj Creative.
en_GBEN