Jacobi Atrophic Vascular Poikiloderma

Jacobian atrophic vascular poikiloderma is a congenital skin disease that is transmitted hereditarily. It usually occurs when two factors combine: congenital and acquired changes that predispose to its development. These include skin hypoplasia and defective differentiation of hair follicle cells. During pregnancy, childbirth and the first year of a child’s life, the functions of the cortex

Jacobi atrophic cycloderma (Java elifort pedicularosa) is also known as atrophic annular lymphoreticulosis. This is an unusual and rare skin condition characterized by the formation of small ring-shaped lesions that may subsequently increase in size. The lesions may be reddish or brown in color and may cover a significant portion of the body surface. The rash usually appears on the back, but can occur on any part of the body. The disease rarely manifests itself with itching and more often with painful sensations in the areas of the rash. Jacobi cycloderma is caused by a virus that is transmitted by contact from an infected person. Predisposition to this disease is associated with weakened immunity and immune disorders. Treatment may include topical creams and ointments, as well as immunotherapy and other methods. But the prognosis is usually good, so these problems can be dealt with quickly using special treatments.