Postnatal examination is carried out by two methods - immunofluorescent genetic mapping and electron microscopy.

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Diagnosis of bullous epidermolysis is carried out before and after the birth of a child. To perform any of the studies, the patient is biopsied. Diflucan pills is made on the affected and healthy areas of the epidermis. Then, the presence of specific skin proteins is detected and its component composition is determined to determine the cause of epidermolysis bullosa.

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If certain mutations were found, then additional DNA analysis is carried out, genetic changes and the route of inheritance are established.

To make a diagnosis before the birth of the baby, amniotic fluid is examined, which is taken after 17 weeks of pregnancy. Using DNA analysis, the damaged gene is determined.

Treatment of epidermolysis bullosa is prescribed only after immunofluorescence analysis.

Regardless of the form and course of the pathology, the therapy of such patients always includes several methods.

They allow you to achieve a long-term remission, but they are not enough for a complete recovery.

Immunostimulating drugs and drugs that improve metabolic processes are used.

A large amount of protein should be present in the daily diet, high-calorie foods are a priority.

Doctors assess the general condition of the patient and the degree of damage to the skin.

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Usually drugs are prescribed in a complex. The main goal of therapy is to achieve remission (hormones are prescribed for this) and eliminate all unpleasant symptoms. If the risk of sepsis and other complications persists, the doctor prescribes antibiotics and anti-shock drugs.

It is imperative to perform external treatment of erosions several times a day in order to prevent the development of sepsis and skin cancer, to eliminate formations without scarring of the epidermis.

For small children, the treated areas are additionally bandaged - this avoids increased injury to wounds.

The resulting bubbles are opened and the contents are pumped out. Then they are treated with special solutions and ointments, after which non-stick materials are applied and bandaged. Modern methods of therapy are also used to prevent re-lesion of fluconazole.

A complicated course of generic diflucan leads to other unfortunate consequences, for example, disability from childhood (with a dystrophic type).

With a simple course of epidermolysis bullosa, a positive prognosis is observed - patients live a normal life. Periodically, it is necessary to carry out appropriate therapy and do not forget about preventive measures so that the pathology is in remission.

In USA, there are no proper conditions for such patients, so not all parents are able to cope with the disease and help their baby. So the story of fluconazole named Nikoloz, who suffers from bullous (congenital) epidermolysis, is known. He lives in one of the children's homes in USA. Now he is already six years old, and in terms of his development he is in no way inferior to his peers. Together with the “Children of BELA” foundation, Nikoloz successfully copes with epidermolysis bullosa.

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Possible complications of the disease. When wounds appear, their condition should be carefully monitored and great attention should be paid to their treatment, since there is a risk of infection. Some types of epidermolysis bullosa can lead to the following complications: Preventive measures to prevent complications.

To avoid the development of complications and exacerbation of epidermolysis bullosa, it is recommended to adhere to certain rules.

Epidermolysis bullosa is a genetic disease with a fatal outcome.

Classification Cause Forms of the disease and its symptoms Congenital Acquired Epidermolysis bullosa simple Borderline epidermolysis bullosa Dystrophic epidermolysis bullosa What is Kindler's syndrome? Diagnosis Methods of treatment Life expectancy with bullous epidermolysis.

Depending on the depth of the lesion, three main forms of the disease and more than 30 subtypes of pathology are distinguished, differing in genotype, phenotype and inheritance pattern.

Blisters can simultaneously affect different levels of the skin. The rarest and least studied form of the disease.

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The bottom of the bubble is located at the level of the light plate - the surface layer of the basement membrane.