Fragile X Syndrome
Fragile X Syndrome Fragile X syndrome is a genetic condition that causes a range of developmental problems, including learning disabilities and cognitive impairment. It is the most common inherited cause of intellectual disability. Causes:- A mutation in the X chromosome's FMR1 gene results in fragile X syndrome. The protein FMRP, which is necessary for brain development, is either absent or decreased as a result of this mutation. Inheritance:- The inheritance pattern for fragile X syndrome is X-linked dominant. This indicates that the disorder can be brought on by a single copy of the mutant gene. Because they only have one X chromosome, males are more likely than females to be impacted. But women can also be impacted, and their symptoms can differ greatly. Symptoms:- Mild to mod...