Summary
A mother in Asheville, North Carolina, discovered her son, Tristan, has Cockayne syndrome, a rare genetic disorder. This syndrome, which causes slow body deterioration and premature aging, affects fewer than 5,000 people in the U.S. Tristan, now 21, stopped growing at age 12 and requires full-time care due to this condition.
Key Facts
- Tristan Burrell stopped growing at age 12 and was later diagnosed with Cockayne syndrome.
- Cockayne syndrome is a rare genetic disorder causing premature aging and growth issues.
- The disorder affects fewer than 5,000 people in the United States.
- Tristan shows symptoms like short stature, tremors, sensitivity to sunlight, and learning difficulties.
- Initially, doctors thought Tristan had a form of autism due to his delayed speech.
- Both of Tristan's parents unknowingly carried the gene for Cockayne syndrome.
- Tristan's condition involves muscle wasting, making everyday activities challenging.
- His mother provides round-the-clock care and has documented their journey on social media.
