Dysplasia Ectodermal Congenital Anhidrotic

Dysplasia ectrodal congenital anhydria is a rare hereditary disease characterized by the presence of underdeveloped skin and lack of sweating. It occurs as a result of a disruption in the development of the skin in the embryonic period. This disease can affect all layers of the skin, including the epidermis, dermis, and sweat gland layer. Treatment for ectrodal congenital anhydria dysplasia includes drug therapy, surgery, and immunotherapy. For a more accurate diagnosis, a number of studies and tests, such as skin biopsies and genetic analysis tests, must be carried out. However, despite advances in the treatment of this disease, dysplasia remains a serious problem in dermatology and requires constant monitoring and skin care. In this article we will look at ectodermal anhydria congenital dysplasia and how to treat it.

Today we will look at a very rare genetic disease that occurs in extremely rare cases - Congenital Skin Dysplasia (Congenital Anaptic Skin Dystrophy). It is caused by the lack of synthesis of a number of regulatory proteins, which causes disturbances in the synthesis of proteins and lipids. This implies the presence of various pathologies in the skin, such as scars, cancer cells, formations, atrophy, uneven distribution of melanin in the body, as well as an excessive tendency to infections.

The first symptom of the disease is pain in the child's abdomen, cramps and vomiting. Also, newborn children have poor hair growth, their