Primary Orthostatic Tremor, also known as Orthostatic Tremor (OT), is a progressive neurological movement disorder, characterized by high-frequency tremors, predominantly in the legs when in a standing position, and an immediate sense of instability. The term “orthostatic tremor” (OT), also Read More …
Category: Musculoskeletal System
Orthostatic Tremor – Causes, Symptoms, Diagnosis, Treatment
Orthostatic tremor is also known as idiopathic orthostatic tremor is a rare disorder characterized by rapid muscle contractions in the legs that occur when standing. People typically experience feelings of unsteadiness or imbalance, causing them to immediately attempt to sit Read More …
Tremors – Causes, Symptoms, Diagnosis, Treatment
Tremors are rhythmic, oscillatory, involuntary movements with muscle contraction disorders leading to shaking movements in one or more parts of the body. It is a common movement disorder that most often affects the hands but can also occur in the Read More …
What is Muscular Dystrophy? – Causes, Symptoms, Treatment
Muscular dystrophy (MD) refers to a group of more than 30 genetic diseases that cause progressive weakness and degeneration of skeletal muscles used during voluntary movement. The word dystrophy is derived from the Greek dys, which means “difficult” or “faulty,” and troph, Read More …
Peroneal Muscular Atrophy – Causes, Symptoms, Treatment
Peroneal Muscular Atrophy/Hereditary Motor and Sensory Neuropathy/Charcot-Marie-Tooth disease (CMT) is slowly progressive neurodegenerative hereditary chronic motor and sensory neuropathy disease and one of a group of disorders that cause damage to the peripheral nerves, the nerves that transmit information and Read More …
Hereditary Motor and Sensory Neuropathy
Hereditary Motor and Sensory Neuropathy/Charcot-Marie-Tooth disease (CMT) is slowly progressive neurodegenerative hereditary chronic motor and sensory neuropathy disease and one of a group of disorders that cause damage to the peripheral nerves, the nerves that transmit information and signals from Read More …
Charcot-Marie-Tooth Syndrome – Causes, Symptoms, Treatment
Charcot-Marie-Tooth Syndrome/Charcot-Marie-Tooth disease (CMT) is slowly progressive neurodegenerative hereditary chronic motor and sensory neuropathy disease and one of a group of disorders that cause damage to the peripheral nerves, the nerves that transmit information and signals from the brain and Read More …
Charcot-Marie-Tooth Hereditary Neuropathy
Charcot-Marie-Tooth Hereditary Neuropathy/Charcot-Marie-Tooth disease (CMT) is slowly progressive neurodegenerative hereditary chronic motor and sensory neuropathy disease and one of a group of disorders that cause damage to the peripheral nerves, the nerves that transmit information and signals from the brain Read More …
Charcot-Marie-Tooth Disease – Causes, Symptoms, Treatment
Charcot-Marie-Tooth disease (CMT) is slowly progressive neurodegenerative hereditary chronic motor and sensory neuropathy disease and one of a group of disorders that cause damage to the peripheral nerves, the nerves that transmit information and signals from the brain and spinal Read More …
What Is Myasthenia Gravis – Causes, Symptoms, Treatment
Myasthenia gravis is a chronic autoimmune, neuromuscular disease that causes weakness in the skeletal muscles that worsens after periods of activity and improves after periods of rest. These muscles are responsible for functions involving breathing and moving parts of the Read More …
Dermatomyositis – Causes, Symptoms, Diagnosis, Treatment
Dermatomyositis is a rare acquired or autoimmune humoral-mediated muscle disease characterized by muscle weakness and a skin rash that causes muscle inflammation and disease condition in which antigen-specific antibodies are deposited in the microvasculature, either secondary to immune complex deposition Read More …
Distal Myopathy and Dysferlinopathy
Distal Myopathy and Dysferlinopathy/Dysferlinopathy include a spectrum of muscle disease characterized by two main phenotypes: Miyoshi myopathy with primarily distal weakness and limb-girdle muscular dystrophy type 2B (LGMD2B) with primarily proximal weakness. Miyoshi myopathy (median age of onset 19 years) Read More …
