6q16 deletion syndrome

Deletion 6q16 syndrome is a Prader-Willi like syndrome characterized by obesity, hyperphagia, hypotonia, small hands and feet, eye/vision anomalies, and global developmental delay.

Also known as: Del(6)(q16), Prader-Willi-like syndrome due to deletion 6q16, monosomy 6q16

0 clinical trials for this condition and its sub-types.