Tag: movement disorders

  • Tremor, Familial

    Tremor, Familial

    Explore the complexities of Familial Tremor, a hereditary neurological condition characterized by rhythmic shaking, primarily in the hands. This blog post delves into its causes, associated symptoms, treatment options, and the importance of early diagnosis, providing essential insights for those affected and their families. Learn how to manage this condition effectively and improve quality of…

  • Rheumatic Chorea

    Rheumatic Chorea: Definition and Description of Rheumatic Chorea: Rheumatic chorea, also known as Sydenham’s chorea, is a neurological disorder characterized by involuntary, rapid, and unintentional movements. It typically manifests as a sequel to rheumatic fever, a complication of untreated streptococcal infections, particularly in children between the ages of 5 and 15 years. The condition affects…

  • Presenile Tremor Syndrome

    Presenile Tremor Syndrome: Definition and Description of Presenile Tremor Syndrome: Presenile Tremor Syndrome is a neurological condition characterized by involuntary shaking or trembling, typically occurring in individuals below the age of 65. This condition can manifest as a primary tremor disorder, often affecting the hands, arms, and sometimes other parts of the body. The tremors…

  • Parkinson’s Disease Center

    Parkinson’s Disease Center: Definition and Description of Parkinson’s Disease Center: The Parkinson’s Disease Center is a specialized facility focused on the diagnosis, treatment, and research of Parkinson’s disease (PD), a progressive neurodegenerative disorder that affects movement control. PD occurs due to the degeneration of dopamine-producing neurons in the brain. This center often provides a comprehensive…

  • Oral-Facial Dyskinesia

    Oral-Facial Dyskinesia: Definition and Description of Oral-Facial Dyskinesia: Oral-Facial Dyskinesia is a condition characterized by involuntary, abnormal movements of the muscles in the face and mouth. This neurological disorder often manifests as repetitive and purposeless movements, including grimacing, lip smacking, and tongue protrusions. The dyskinesia can result from various factors, including long-term use of certain…

  • Linguofacial Dyskinesia

    Linguofacial Dyskinesia Definition and Description of Linguofacial Dyskinesia Linguofacial Dyskinesia is a neurological condition characterized by involuntary movements of the muscles in the face and mouth. This disorder often manifests as repetitive, distal movements and can significantly impact an individual’s ability to speak, chew, and perform other essential functions. The term ‘dyskinesia’ refers to abnormal,…

  • Idiopathic Basal Ganglia Calcification

    Idiopathic Basal Ganglia Calcification Idiopathic Basal Ganglia Calcification Definition and Description of Idiopathic Basal Ganglia Calcification Idiopathic Basal Ganglia Calcification (also known as Fahr’s syndrome) is a rare neurological condition characterized by abnormal calcium deposits in the basal ganglia, which are clusters of nerve cells responsible for regulating movement. The term “idiopathic” indicates that the…

  • Huntington’s Disease (HD)

    Huntington’s Disease (HD) Definition and Description of Huntington’s Disease (HD) Huntington’s Disease (HD) is a progressive neurodegenerative disorder caused by a genetic mutation in the HTT gene. This mutation leads to the production of a toxic protein, which gradually damages brain cells, particularly in areas that control movement, mood, and cognition. The condition typically manifests…

  • FRAXA

    FRAXA Definition and Description of FRAXA FRAXA (Fragile X-Associated Tremor/Ataxia Syndrome) is a neurological disorder that affects individuals carrying the fragile X premutation. This condition primarily manifests with movement disorders, tremors, and ataxia (lack of muscle coordination). Patients often experience a range of symptoms that can impact daily functioning, and it is linked to the…

  • Fahr Disease

    Fahr Disease Definition and Description of Fahr Disease Fahr Disease, also known as Fahr’s Syndrome, is a rare neurological disorder characterized by the abnormal accumulation of calcium in areas of the brain known as the basal ganglia. This condition can lead to various neurological and psychiatric symptoms. The exact mechanism of calcium deposition is not…