Frankl-Hochwart Syndrome

Frankl-Hochwart syndrome: causes, symptoms and treatment

Frankl-Hochwart syndrome is a rare neurological disease that was named after the Austrian neurologist Ludwig Frankl-Hochwart, who first described the disease in 1891. The syndrome is characterized by dysfunction of the nervous system, which leads to impaired coordination of movements and decreased muscle strength.

The causes of Frankl-Hochwart syndrome are not fully understood, but it is known that the most common cause is heredity. In some cases, the syndrome may be caused by injury or infection of the nervous system.

Symptoms of Frankl-Hochwart syndrome can manifest themselves in varying degrees of severity, depending on the individual characteristics of the patient. One of the main symptoms is ataxia - a lack of coordination of movements, which leads to instability when walking and other motor activities. Patients may also experience neurological weakness, including decreased muscle strength and reflexes, and sensory problems.

Diagnosis of Frankl-Hochwart syndrome includes a neurological examination, a study of medical and family history, as well as various laboratory and instrumental research methods, such as magnetic resonance imaging (MRI) and electromyography (EMG).

Treatment for Frankl-Hochwart syndrome is aimed at improving symptoms and preventing complications. There is currently no specific therapy for this condition, but symptoms can be improved with physical therapy, medications to improve muscle function and reflexes, and medications such as antidepressants and anticonvulsants.

Overall, Frankl-Hochwarth syndrome is a rare but serious disease that requires careful monitoring and comprehensive treatment. If you suspect this syndrome, contact a neurologist for consultation and diagnosis.

Frankl Hochwart named a complex of symptoms that manifest themselves in a significant proportion of elderly patients due to atherosclerosis, as well as various blood diseases. Clinically, dementia rapidly develops; treatment requires observation and nutritional correction.

**Definition of the syndrome** F.-H. syndrome is based on the general clinical picture of dementia in patients over 50 years of age, which is characterized by: - ​​late development (from one to several years). - memory impairment, depending on the patient’s daily routine. — relationship of the disease with impaired hemostasis; - history of gastrointestinal pathology; - epileptic seizures throughout life (about