📂 Diseases
neuronopathy, distal hereditary motor, type 7A — Definition
Distal herediter motor nöronopati tip 7A / neuronopathy, distal hereditary motor, type 7A
Distal herediter motor neuronopathy type 7A is a neurodegenerative disease that affects the motor neurons of the peripheral nervous system, autozomal dominant inheritance. The disease is characterized by weakness and atrophy in dystal muscles, especially like hands and feet, but sensory loss is not pronounced. Symptoms often begin in the adult period and can spread to proximal muscles over time. Genetic mutations (e.g. HSPB1 or HSPB8 genes) lead to the disease by disrupting the disruption of motor neurons.
Frequently Asked Questions
❓ What is Distal herediter motor nöronopati tip 7A?
Distal herediter motor nöronopati tip 7A; distal herediter motor neuronopathy type 7A is a neurodegenerative disease that affects the motor neurons of the peripheral nervous system, autozomal dominant inheritance. The disease is characterized by weakness and atrophy in dystal muscles, especially like hands and feet, but sensory loss is not pronounced. Symptoms often begin in the adult period and can spread to proximal muscles over time. Genetic mutations (e.g. HSPB1 or HSPB8 genes) lead to the disease by disrupting the disruption of motor neurons.
❓ What is neuronopathy, distal hereditary motor, type 7A in Turkish?
The Turkish equivalent of "neuronopathy, distal hereditary motor, type 7A" is Distal herediter motor nöronopati tip 7A.
❓ Which medical field is Distal herediter motor nöronopati tip 7A related to?
This term belongs to the Diseases category.