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Stories are written for and by people around 3q29 microdeletion syndrome, so we know what we are talking about. We listen to all the stories, write them down and share them. And translate relevant news about 3q29 microdeletion syndrome into readable articles. In this way we want to connect families, let them laugh and relax or give them just that little bit of support.

Because if there is something important for families with a care-intensive person like 3q29 microdeletion syndrome, it is that the family remain upright. And that is what we, as community around 3q29 microdeletion syndrome, are committed to doing with heart and soul.

3q29 microdeletion syndrome is a rare chromosome disorder. Symptoms may include delay reaching some developmental milestones such as sitting, walking or talking, frequent ear and respiratory infections, and a small head size (microcephaly). Some babies with this condition are born with a cleft lip or cleft palate, and a few have been reported to have heart defects. As children with this condition get older, they may develop behavioral difficulties such as autism, and they may have symptoms of mental illness.[1] The severity of symptoms can vary, and some people with 3q29 microdeletion syndrome may have very mild symptoms or may not even know they are affected.[2] 


 

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