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From: Maria W.
Date: 09 Oct 2011
Time: 20:13:27 -0500
Remote Name: 68.119.36.221
“Careful clinical examination of a small sample of people who stutter who carry mutations in these genes has failed to identify any symptoms of MLII or MLIII.” Does the same hold true for children diagnosed with this rare disorder showing any signs of stuttering? Do they have a genetic predisposition (i.e. a family member who stutters) to stuttering?