Stichting Rubinstein-Taybi Syndroom

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Rubinstein-Taybi syndrome

Rubinstein-Taybi syndrome is a condition characterized by short stature, moderate to severe learning difficulties, distinctive facial features, and broad thumbs and first toes. It occurs in an estimated 1 in 125,000-300,000 births.

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Avez-vous besoin d'aide ?

Vous êtes nouveau ici ? Vous vous sentez dépassé ? Alors commencez par le début, et laissez-nous vous présenter le SRT étape par étape.

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Histoires d'expérience

Share your stories and hear those of others

RTS is a long journey; sometimes difficult but often you arrive at a sunny place. Talking about it helps you cope with the journey.

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Meeting others

There are others in the same situation as you. If you connect with us we can help you find them. Maybe you want to meet someone with similar experiences.

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Demander à l'expert

Ask our experts

We all have questions on the care and wellbeing of our loved ones with RTS. Search the questions others have asked before. No question is too big or too small to ask.

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Comunauté

Onze opdracht

"Wij zetten ons in om bij te dragen aan een accurate diagnose van problemen bij mensen met Rubinstein Taybi, om onderzoek naar aspecten van Rubinstein Taybi te ondersteunen, om mensen met Rubinstein Taybi te helpen en om hun ouders, broers en zussen, grootouders, families, verzorgers en artsen te helpen weloverwogen beslissingen te nemen."

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Notre vision

Our movie

Rubinstein-Taybi Syndrome (RTS) is difficult to understandThe best way to find out is by watching our introductory video.

Rubinstein-Taybi syndrome à léchelle mondiale