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Mitochondrial DNA-associated Leigh Syndrome: Understanding the Disease 1. Introduction Mitochondrial DNA-associated Leigh Syndrome, often referred to as Leigh Syndrome, is a rare, inherited, progressive neurological disorder that usually becomes apparent in infancy or early childhood. It is characterized by a progressive loss of mental and movement abilities (psychomotor regression) and typically results in devastating complications….
Epilepsy: Understanding the Condition and Living with It 1. Introduction Epilepsy is a neurological disorder characterized by recurrent seizures. These seizures are caused by abnormal electrical activity in the brain and can vary from brief lapses of attention to severe and prolonged convulsions. 2. Symptoms The symptoms of epilepsy can range from staring spells and…
Understanding Brain Dopamine-Serotonin Vesicular Transport Disease 1. Introduction Brain Dopamine-Serotonin Vesicular Transport Disease, also known as DTDS, is a rare genetic neurological disorder that affects the transport of dopamine and serotonin in the brain. This condition disrupts the proper packaging and release of these neurotransmitters, leading to a range of neurological and psychiatric symptoms. 2….
Aphasia: Understanding the Language Disorder Introduction Aphasia is a language disorder that impairs a person’s ability to communicate. It is often caused by damage to the brain, usually from a stroke or head injury. Individuals with aphasia may have difficulty speaking, understanding speech, reading, and writing. This condition can be frustrating and challenging, impacting various…
Understanding Adult Neuronal Ceroid Lipofuscinosis: A Comprehensive Guide Introduction Adult Neuronal Ceroid Lipofuscinosis (ANCL) is a rare, progressive neurological disorder that primarily affects adults. Also known as Kufs disease, ANCL is characterized by the abnormal accumulation of lipopigments in the body’s tissues, including the brain and other organs. This condition leads to a decline in…