Fatal Familial Insomnia (FFI) is a rare genetic disorder that affects the sleep-wake cycle. It is not contagious and cannot be transmitted from person to person through contact or exposure. FFI is caused by a mutation in the PRNP gene and is inherited in an autosomal dominant pattern. The disease leads to progressively worsening insomnia, followed by other neurological symptoms. FFI is a genetic condition and can only be passed down from affected individuals to their offspring.
Fatal Familial Insomnia (FFI) is an extremely rare and devastating genetic disorder that affects the sleep-wake cycle. It is characterized by progressively worsening insomnia, leading to a complete inability to sleep. FFI is caused by a mutation in the PRNP gene, which is inherited in an autosomal dominant pattern.
While FFI is a genetic disorder, it is not contagious. It cannot be transmitted from person to person through any form of contact or exposure. The mutation responsible for FFI is passed down from affected individuals to their offspring through their genes.
It is important to note that FFI is an inherited condition, meaning that individuals who have a family history of the disorder are at a higher risk of developing it themselves. However, not everyone with the mutated gene will necessarily develop FFI, as the onset and severity of the disease can vary.
Due to the extremely rare nature of FFI, with only a few hundred cases reported worldwide, it is crucial for individuals with a family history of the disorder to seek genetic counseling and testing if they are concerned about their risk.