Recklinghausen's Disease

Problems and current aspects of the study of Recklinghausen's disease

**Recklinghausen's disease** is a rare complex hereditary autosomal dominant connective tissue disease characterized by a triad of pathological signs: skeletal deformities, characteristic changes in the facial skeleton and finger deformities. Due to weak clinical and pathogenetic substantiation, the disease was not included in the WHO nomenclature of diseases for a long time. The problem is due to insufficient understanding of the etiology, the morphology is practically unstudied, and the clinical picture has certain individual differences. Diagnosis is difficult due to the lack of specific diagnostic methods. A modern complex of laboratory tests, as well as imaging research methods, makes it possible to identify the pathological pathomorphology of connective tissue both when this disease is suspected and at its subsequent stages.

The disease manifests itself after two to three years of life (with maximum manifestation usually at the age of 6-7 years) and has a very slow, steadily progressive course with the threat of deformation of the vertebrae, ribs, spine, deformation of the joints, shortening of the fingers and toes. Narrowing of the cerebral canal and cerebellum, downward displacement of the eye, lengthening of the nose, clefts of the upper lip, etc. are observed.

It is generally accepted that this is a form of juvenile osteo

There is such a type of mental disorder - Recklinghausen disfluent (dissociative) hysteria. Although this syndrome itself was described back in 1887 by the German pathologist Friedrich David Recklinghausen, the scientific community “calculated” this diagnosis quite recently - several years ago, and as an independent mental disorder, and not one of the forms of exotic mental pathology .

*Dissoziative Störungen* Currently, this type of mental disorder affects 5 to 7% of the population. Patients may experience a variety of symptoms (for example, strange memories, feelings of split personality, or bouts of hallucinations). This pathology is often associated with mental disorders and the manifestation of symptoms such as panic attacks, anxiety attacks and obsessive fears.

Psychological stress and other psychological factors play an important role in the occurrence of this syndrome. Genetic and biological factors, as well as social and cultural factors, may also be important.

The cause of the disorder is functional disturbances in the functioning of the brain. Its receptors stop processing information correctly - as a result, we lose awareness of what is being suggested to us from the outside, what surrounds us.

Such patients do not perceive the voices of other people if they address them by name. Most often, they do not respond to calls and generally cannot understand the surrounding situation during an attack. At the moment of its onset, patients “split into two” or, on the contrary, “become like others.”

Symptoms and complaints for different types of dissociative amnesia will not be the same. This is precisely what does not allow an accurate diagnosis to be made when talking with the patient. Sometimes, in order to finally establish a diagnosis of a disorder, it is necessary to conduct additional examinations and consult with specialists.

The discovery and description of a disease called “Recklinghausen disease” is one of the most significant discoveries in the world of medical science today. This disease affects the human nervous system, leading to serious disorders of the brain and mental disorders. Below is an article about the discovery of Recklinghusen's disease and its clinical manifestations:

The discovery of Recklinghausen's disease is one of the most important achievements of medical science of the twentieth century. It was discovered in 1868 by the German pathologist Friedrich Didlert Recklinghausen, and was named after the scientist. Recklenhausen's disease or Recklinghausin's disease, the second and more common name is diaphyseal hernia, is accompanied by the formation of semi-bridge-like tumors - diverticula, which are protrusions of internal

A little about the author and the disease.

Hans Paul Rekelinghaus is a German physician, member of the Göttingen Academy of Sciences and professor of pathological anatomy, also known for his work on Gröbfeld syndrome. Hans lived from 1849 to 1926. He was born in Germany, in the city of Arnstadt, and died during the First World War. The subject of his medical research was "anencephaly" and "developmental delay". He considers himself the founder of this kind of disease. It is also worth mentioning that Reckel's disease, that is, Gröbel's syndrome