Paroxysmal Kinesigenic Choreathetosis / Dyskinesia (PKC/D) is not contagious.
PKC/D is a rare neurological disorder characterized by sudden, brief episodes of abnormal involuntary movements triggered by sudden movements. It is considered a genetic condition caused by mutations in certain genes.
PKC/D is not transmitted from person to person through contact or exposure. It is an inherited disorder, meaning it can be passed down through families, but it is not contagious in the traditional sense.
Paroxysmal Kinesigenic Choreathetosis/Dyskinesia (PKC/D) is a rare neurological disorder characterized by sudden, brief episodes of involuntary movements. These episodes, known as paroxysms, can be triggered by sudden movements or changes in posture. While PKC/D can be distressing for those affected, it is important to note that it is not contagious.
PKC/D is considered a genetic disorder, meaning it is caused by specific genetic mutations. It is typically inherited in an autosomal dominant manner, which means that an affected individual has a 50% chance of passing the condition on to their children. However, not all individuals with PKC/D have a family history of the disorder, as spontaneous mutations can also occur.
The exact mechanisms underlying PKC/D are not fully understood, but it is believed to involve abnormalities in the brain's movement control centers. These abnormalities can lead to the sudden, involuntary movements characteristic of the disorder.
It is important to note that PKC/D is a neurological condition and not an infectious disease. It cannot be transmitted from person to person through contact or exposure. Therefore, individuals with PKC/D do not pose any risk of contagion to others.