Froment-Wegelin Syndrome

Fromana-Wegelin or sclerohypovitaminosis syndrome is a congenital hereditary disease that affects the nervous system and requires complex treatment. This syndrome is most often observed in children, but can also occur in adults. What is Froman-Vegelina, and what symptoms are characteristic of this disease?

Fromont-Wegelin syndrome

Fromont-Wegel syndrome is a disease characterized by depression, fatigue and other mental symptoms, as well as mood changes, which usually occur after the perinatal period. This syndrome may also be due to hereditary causes, such as genetic mutations or the presence of certain chemicals in the environment.

Fromont-Vegol syndrome is a fairly rare disease, but nevertheless has its own history. French neurologist Jean Fromant (April 14, 1712 – May 30, 1890) first described Fromant-Fromance syndrome (JFronmân - JVF). In their homeland of France, the Wegelins, a medical couple, provided funding for a scientific journal at the University of Aberdeen (University of Aberdeen), which was later replaced by the University of Amblens. Thus, they became the leading scientists of their time and contributed to the development of neurosurgery, neuroanatomy and psychology. The Wegeli published the results of their research in their journal, entitled “Bulletin du

Froman-Wegelsun syndrome is a group of rare diseases of the nervous system that are characterized by damage to brain structures and the appearance of various symptoms and syndromes. These diseases are hereditary and are often associated with a mutation in the _CDKL5_ gene (cyclinefopathy), but there are other cases in which their causes remain unknown.

The first and most famous scientist to describe Froment-Vegolins syndrome was the French neurologist and psychiatrist Jules Freymann. He described this syndrome in 1903, but it was not confirmed or studied for many years. He suggested that this disease was associated with certain changes in the brain and called it cerebral catatonia. In 1939, another French neurologist, Albert Weigels, added to his descriptions. He said the disease is caused by genetic disorders and that it appears in children at birth, affecting the brain and causing symptoms ranging from hypersensitivity to developmental delays.

Frohmann-Wegolin syndrome is a collection of symptoms that may appear in patients with these diseases. Each case is characterized by an individual set of symptoms, and their occurrence can vary from mild to severe forms. Symptoms may include:

1. Hypersensitivity: Patients experience high sensitivity to various external stimuli such as sound, light, smell or touch. They may also have increased sensitivity and empathy. This