Fragile X syndrome
Fragile X syndrome is a genetic condition involving changes in part of the X chromosome.This condition causes a range of developmental problems including learning disabilities and cognitive impairment. It is the most common form of inherited intellectual disability in males and a significant cause of intellectual disability in females.
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Original Article Posted on: NA
Link to Original Article: https://rarediseases.info.nih.gov/diseases/6464/fragile-x-syndrome