What is Paroxysmal Kinesigenic Choreathetosis / Dyskinesia

Paroxysmal Kinesigenic Choreathetosis/Dyskinesia (PKC/D) is a rare neurological disorder characterized by sudden, brief, and involuntary movements. These movements, known as chorea, are often triggered by sudden movements or changes in posture. PKC/D typically starts in childhood or early adulthood and can persist throughout a person's life.

During an episode, individuals with PKC/D may experience jerking or twisting movements in their limbs, face, or trunk. These episodes can last from a few seconds to a few minutes and may occur multiple times a day. The frequency and severity of the episodes can vary among individuals.

The exact cause of PKC/D is not fully understood, but it is believed to be related to abnormal electrical activity in certain areas of the brain. In some cases, PKC/D may be inherited through a genetic mutation.

While PKC/D can be disruptive and distressing, it is generally not life-threatening. Medications, such as anticonvulsants, can help manage the symptoms and reduce the frequency of episodes. With proper treatment, individuals with PKC/D can lead relatively normal lives.

Paroxysmal Kinesigenic Choreathetosis/Dyskinesia (PKC/D) is a rare neurological disorder characterized by sudden, brief, and involuntary movements triggered by sudden movements or changes in posture. These episodes of chorea can occur multiple times a day and last from a few seconds to a few minutes. While the exact cause is unknown, it is believed to involve abnormal brain activity. PKC/D can be managed with medications, allowing individuals to lead relatively normal lives.