käsimärt
Käsimärt is a rare, inherited neurological disorder that affects the peripheral nervous system. It is characterized by progressive muscle weakness, sensory loss, and autonomic dysfunction. The onset of symptoms typically occurs in early adulthood, though it can manifest earlier or later in life. The exact prevalence of käsimärt is unknown due to its rarity.
The primary symptoms of käsimärt include distal limb weakness, particularly affecting the hands and feet, which
Käsimärt is caused by mutations in specific genes that are essential for the development and maintenance of
Currently, there is no cure for käsimärt. Treatment focuses on managing symptoms and improving quality of life.