Weber-Hübler-Jandren syndrome

Weber-Hübler-Gendrin syndrome: a rare neurological disorder

Weber-Hübler-Gendrin syndrome (GJS) is a rare neurological disease named after three doctors who made significant contributions to its research and description: German physician Wilhelm Eduard Weber (1823-1918), French physician Henri Hübler (1821-1879) and the French physician Antoine Nicolas Gendrin (1796-1890).

Weber-Hübler-Gendrin syndrome is characterized by damage to the nerve structures responsible for motor functions and innervation of the face. It usually presents with unilateral weakness or paralysis of half the face, as well as associated symptoms such as sensory disturbances and pain.

This syndrome is caused by damage to the facial nerve, which is responsible for the motor function of the face. Damage can be caused by a variety of factors, including inflammation, tumors, vascular disorders and trauma. Depending on which part of the nerve is affected, symptoms can range from mild to severe.

The main signs of Weber-Hübler-Gendrin syndrome include asymmetrical drooping of the corner of the mouth, difficulty closing the eye, weakness of the facial muscles, changes in taste, and increased sensitivity to sounds. Some patients may experience pain in the ear or face.

To diagnose Weber-Hübler-Gendrin syndrome, doctors usually rely on clinical manifestations and the results of a neurological examination. In addition, additional tests, such as electromyography and various educational methods, may be required to assess the extent of the damage and determine the cause of the syndrome.

Treatment of Weber-Hübler-Gendrin syndrome is aimed at eliminating the underlying cause of damage to the facial nerve. In some cases, physical therapy, massage, and medications may be necessary to relieve symptoms and speed up recovery of facial muscles.

In general, Weber-Hübler-Gendrin syndrome is a rare and poorly understood disease. Thanks to the work of Weber, Gubler and Gendren, we were able to gain more information about its characteristics and approaches to diagnosis and treatment. However, further research is required to better understand this syndrome and develop effective treatments for it.

In general, Weber-Hübler-Gendrin syndrome is a rare neurological disorder characterized by damage to the facial nerve and manifested by unilateral weakness or paralysis of the facial muscles. Timely diagnosis and comprehensive treatment play an important role in improving the prognosis and quality of life of patients suffering from this syndrome.

Weber-Hübler-Gandren syndrome

Weber-Gübler-Jendren syndrome (Weber syndrome, NRC - Wieber Syndrome, English Weer-Gübler-Jendren, Weir-Güberein-Sindromen) also called Anglo-French syndrome. Weber - Gübler - Gendre in honor of the authors of the proposed treatment methods. It was initially described as an independent disease. Each patient is identified with abnormal facial features, accompanied by visual impairment.

The syndrome is also called deaf-deaf, Addison's, Avadero - while the name of the author who first described it is either Herbert Avadero or Avaedern, which confuses researchers. Sometimes the syndrome is called "Weberian pits" ("pit syndrome") or "Weberian cri"

Weber-Hübler-Gandren syndrome: history and current state of the problem

For the first time, the famous pathologist Professor of the St. Petersburg Academy Nikolai Mikhailovich Schmidt, together with Professor Ivan Grigorievich Savchenko, spoke about Weber-Hütler syndrome in 1924.

Main clinical symptoms: fever against the background of subcutaneous hemorrhages in various organs, which manifest themselves in the form of marbled reticulation of the skin, sweating, microcirculation disorders, necrosis of the superficial layers of the skin, multiple pinpoint hemorrhages, lymphoid hyperplasia of the meninges, generalized lymphadenitis