1. Hutchinson-Gilford progeria syndrome
If you are a social media addict, like many of us are nowadays, you have probably heard of this syndrome because you have read the story of Adalia Rose. Adalia is 1 in 4 million children worldwide who was diagnosed with progeria syndrome. Given that it is so rare, progeria occupies the 1st place on our list of 10 uncommon genetic mutations in humans. Children who have the condition have an appearance of rapid aging. They also develop hair loss, joint abnormalities and a loss of fat under the skin.
This was Insider Monkey’s list of 10 uncommon genetic mutations in humans.