Ring chromosome 16

Ring chromosome 16 is characterized bypostnatal growthdeficiency, intellectual disability, microcephaly, broad flat nasal bridge, down-turned mouth, low-set and dysmorphic (abnormally-shaped) ears and speech delay.To date, less than 10 cases have been reported in the medical literature.

Also known as: Ring chromosome type 16, R16, Ring 16, Ring chromosome 16 syndrome, chromosome 16 ring

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