Feits
Feits, also known as *Feitsma* or *Feitsma’s disease*, is a rare genetic disorder characterized by progressive neurological degeneration. The condition primarily affects the cerebellum, leading to ataxia (loss of coordination), dysarthria (difficulty speaking), and other motor impairments. It is classified as a type of spinocerebellar ataxia (SCA), a group of inherited disorders that disrupt the nervous system.
Feits was first described in the early 20th century by Dutch neurologist Dr. Jacob Feitsma, who documented
Symptoms of Feits usually begin in early adulthood, often between the ages of 20 and 40, and
Diagnosis involves a combination of genetic testing, neurological examinations, and imaging studies such as MRI scans
Feits is considered a rare condition, with only a few hundred documented cases worldwide. Research efforts