What is Rubinstein Taybi Syndrome (RTS)?
RTS is a rare syndrome. It refers to a specific pattern of physical features and developmental disabilities, which occur together in a consistent fashion. Individuals with RTS have short stature, developmental delay, similar facial features, and broad thumbs and first toes. (Stevens & Carey, 1991) What causes RTS? The cause of RTS is unknown and there is no reason to believe that anything the parents did or did not do during pregnancy caused the child to have RTS. (Stevens & Carey, 1991) If I have another child, will that child have RTS? It is highly UNlikely. There is less than 1% chance of having another child with RTS. Are there medical tests to specifically diagnosis RTS? No, RTS is diagnosed by specific physical characteristics. A genetist or other medical professional will make the diagnosis. Is there a cure? There is not a cure at this time. Currently, research is being conducted to identify the chromosome involved with RTS. What medical issues can I expect? It is important to u