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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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Do you need help
Are you new here? Do you find it overwhelming? Start at the beginning and let us, step by step, guide you and introduce you with Rubinstein Tayby Syndrome.
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Raoul Hennekam
Above all, share information and experiences with each other. Everyone has a little information and all these little bits become a wealth of information. Hugely valuable.
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.
Lesen...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.
Lesen...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.
Lesen...missie
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.
Lesen...Our movie
Rubinstein-Taybi Syndrome (RTS) is difficult to understandThe best way to find out is by watching our introductory video.
