Rett Syndrome
Rett Syndrome is a neurological disorder that primarily affects females. It is a genetic disorder caused by a mutation in the MECP2 gene located on the X chromosome. It is characterized by normal early development followed by loss of purposeful hand use, slowed head growth, problems with walking, recurrent breathing pauses, seizures, and social and communication impairments. Rett Syndrome is a rare disorder, affecting around one in every 10,000 to 23,000 female births. Early diagnosis and intervention can lead to improved outcomes. There is no cure for Rett Syndrome, but treatments and lifestyle adjustments can help manage symptoms and improve quality of life.
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