Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Ring chromosome 16

MONDO:0019909

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

0 clinical trials for this condition and its sub-types, 0 tagged with Ring chromosome 16 itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.