Thanks to you, Alyosha will soon receive the results of a detailed DNA study!

Alyosha is 11 years old. At birth, the boy was diagnosed with Cruson's syndrome. This rare genetic disease, due to which the skull is deformed, was transmitted from the father. The boy had his first operation at the age of 3 months. But this was not enough. The fontanelles overgrown very early, so Alyosha's head almost does not grow. The brain and facial part of the skull are severely deformed. Alyosha is already accustomed to operations and is sympathetic to what is different from others. The boy goes to school, attends physical education classes, although he does not always cope with the load. In July 2022, Alyosha underwent a genetic analysis - Cruson's syndrome was not confirmed. Then the doctors ordered a full genome sequencing (a detailed study of DNA). This will determine the exact cause of the disease and find "broken" genes. Help our ward so that doctors can make an accurate diagnosis. Without this, it is impossible to choose the right treatment and predict the consequences of mutations.