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In severe cases, they are formed in the organs of the genitourinary system, intestines and esophagus. Possible death. Dystrophic. Clinical manifestations differ depending on the type of inheritance. Diseases with a recessive type of imitrex pill are characterized by the formation of blisters in the esophagus, the fusion of fingers and toes, and an increased risk of skin cancer. Diseases with a dominant type of inheritance are manifested by the appearance of blisters on the skin in the area of the elbow and knee joints, on the mucous membranes.

Healing of burst blisters occurs without scarring. Immediately after birth, a generalized hemorrhagic rash appears on the skin and mucous membranes of the child. After opening the bubbles, long-term non-healing erosions form in their place. Accession of a secondary pyogenic infection causes the development of sepsis and death of the newborn.

Diagnosis of bullous epidermolysis can be prenatal (before the birth of a child) and postnatal (after birth). Prenatal diagnosis is based on a genetic analysis of amniotic fluid obtained during an amniocentesis performed after the 17th week of pregnancy.

If genetic mutations characteristic of severe forms of epidermolysis bullosa (malignant, dystrophic) are detected in the fetus, a couple is recommended to buy sumatriptan online the pregnancy for medical reasons.
An important role in the diagnosis of epidermolysis bullosa is played by DNA analysis. It allows you to identify the localization of the mutated gene, as well as determine the type of inheritance of the disease.
There is no specific treatment for epidermolysis bullosa, treatment is symptomatic. The main efforts are aimed at preventing injury to the skin, as well as preventing the addition of a secondary pyogenic infection.
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