MSL2 syndrome
Hi everyone, at first sorry for my english I didn't write for a long time and I live now in Germany.
Our 7 years old son has after cca 5 years finally diagnose (many mixed disorders). They have found by genetic tests rare disorder which calls MSL2 syndrome (I have found as Karayol-Borroto-Haghshenas Neurodevelopmental Syndrome). Doctor in genetic ambulance saied me, that it has only few people on all the world.
Have you someone experiences with this syndrome?
, welcome, we're glad you're here with us. I am hoping that someone in the community can jump in with some knowledge of this syndrome. Please know that we'll always be here to share support. - Warmly, Donna (Team Member)
