A rare degenerative neurological disorder characterized by abnormal calcium deposits and associated cell loss in certain areas of the brain, such as the basal ganglia. Symptoms include progressive deterioration of cognitive abilities leading to dementia and loss of acquired motor skills.
Fahr’s disease is a rare and progressive neurological condition. It is identified by the presence of unusual calcium deposits and linked to cell death in certain parts of the brain. This disease can be hereditary, exhibiting either an autosomal recessive or autosomal dominant inheritance pattern. However, in many instances, the root cause of the disorder remains unidentified. Please note, this is written in English.
Signs of Fahr’s disease encompass progressive dementia, which is the decline in brain function, and the loss of previously learned motor skills. Patients may also experience escalating muscle rigidity and limited mobility. Potential complications can manifest as athetosis, defined by slow, involuntary, twisting movements, or chorea, defined by irregular, quick, jumpy movements. A steady decline in vision may also occur. Please note, this is written in English.
The specific symptoms of Fahr’s disease can be managed as they arise, however, there is currently no known cure for the condition.