SPW Brasil

Brazilian Prader-Willi Syndrome Association

Supporting families and individuals with PWS for over 10 years

What is Prader-Willi Syndrome?

PWS is a rare genetic disorder affecting approximately 1 in 15,000 births. It is characterized by hypotonia at birth, feeding difficulties in infancy, and later hyperphagia (insatiable hunger) that can lead to obesity.

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How We Can Help

Free Diagnosis

Free molecular testing through IFF/FIOCRUZ.

Family Support

Support network and information for affected families.

For Professionals

Educational materials for healthcare professionals.

Events & Meetings

Lectures and workshops with specialists.

600+

Diagnosed

900+

Families Supported

Years of Service

Countries Reached

Precisa de Ajuda?

Faça nossa triagem online para entender se seu filho pode ter sinais da Síndrome de Prader-Willi. O diagnóstico precoce é fundamental para o tratamento adequado.

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