Table of Contents What is Status Epilepticus? Status epilepticus (SE) is a life-threatening neurological emergency where seizures last longer than 5 minutes or recur rapidly without recovery. It affects 10–40 per 100,000 […]
Table of Contents 1. What Are Febrile Seizures? Febrile seizures are convulsions triggered by a sudden spike in body temperature (usually >100.4°F/38°C) in children aged 6 months to 5 years. They […]
Comprehensive Guide to Infantile Spasms (West Syndrome): Expert Care from Cuttack’s Top Neurologist Table of Contents 1. Understanding Infantile Spasms Infantile spasms, also known as West syndrome, is a rare […]
Comprehensive Guide to Lennox-Gastaut Syndrome (LGS): Expert Care in Cuttack Lennox-Gastaut syndrome (LGS) is a rare, severe form of childhood-onset epilepsy characterized by multiple seizure types, cognitive impairment, and significant […]
Table of Contents What is Dravet Syndrome? Dravet syndrome, formerly known as Severe Myoclonic Epilepsy of Infancy (SMEI), is a rare, catastrophic form of epilepsy caused by a genetic mutation […]
Comprehensive Guide: Expert Care from Cuttack’s Leading Neurologist It is a complex neurological condition affecting millions worldwide, characterized by recurrent seizures. Early diagnosis and expert care are critical to managing […]
Table of Contents 1. What Is Dermatomyositis? Dermatomyositis is a rare inflammatory disease causing muscle weakness and skin rashes. It belongs to the group of autoimmune disorders where the immune system attacks healthy muscle […]
Table of Contents 1. What Is Polymyositis? Polymyositis is a rare inflammatory disease that causes muscle weakness due to chronic muscle inflammation. It primarily affects proximal muscles (shoulders, hips, and […]
Table of Contents 1. What Is Charcot-Marie-Tooth Disease-CMT? Charcot-Marie-Tooth Disease-CMT is a hereditary neurological disorder that damages peripheral nerves, leading to muscle weakness, foot deformities, and sensory loss. Named after […]
Table of Contents 1. What Are Muscular Dystrophies? Muscular Dystrophies are a group of genetic disorders characterized by progressive muscle weakness and degeneration. These conditions are caused by mutations in […]
