Albinism

**Albinism. Classification, etiology, pathogenesis and treatment of albinism

Congenital albinism (albinosim congenitum)** is a disease from the group of albinisms in which melanins are absent and skin hypomelanosis is characteristic.

It is extremely rare, its frequency is 1

The manifestations of albinism are extremely diverse and are the result of various gene mutations in the HERC2 gene. This disease is characterized by problems with the metabolism of melanin, which is responsible for skin and hair color. As a result of the anomaly, a person's skin becomes pink or pale, and hair and eyes become colorless. Intelligence