Thank you for helping Timur with the cost of the analysis!

Immediately after birth, Timur was diagnosed with corneal opacity. The boy can see, but very poorly. Nevertheless, he navigates well at home and can find large toys, but he goes outdoors only when accompanied. Timur also attends a kindergarten where the same children with special needs are engaged with specialists. Timur has a visual disability. In 2022 Timur was sent to the Federal State Budgetary Institution “Helmholtz Eye Diseases Research Center. Helmholtz” of the Ministry of Health of Russia, the family hoped for an operation. But they were refused because they could not give guarantees of a good result. Timur's vision problems are hereditary, his mother has had cataracts since birth (disability), but the loss of vision is not so pronounced. Vision is not the only problem that bothers Timur and his family. The boy is hard of hearing and hardly speaks at all. Recently he has learned the word “mom”. If he needs something, he shows it. Mom is very worried that Timur does not speak. Genetic analysis will help to find out the causes of this problem and possibly help with its solution. Please support Timur!