To overcome the delay in the development of Alzhanat, a genetic analysis must be performed

Aljanat, 4 years old, is Aizanat's twin sister. During the 35th week of pregnancy, the girls' mother contracted COVID-19. From birth, they lag behind in development. The twins have the same diagnoses: genetically unverified myopathic syndrome, neuropsychiatric and speech development disorder (level 2 OHD) with behavioral disorders. ICD-10 code: G71.9, F83, F90, and M21.4 — flat hallux valgus and hyperactive syndrome. Since the age of one, girls have been undergoing rehabilitation 2-3 times a year, but so far there has been no improvement. Nevertheless, their mother does not give up and does everything possible for their health. Currently, the Dean's office needs to undergo a genetic blood test with full genomic sequencing at the Bochkov Medical and Genetic Center in Moscow to identify a complex disease - unverified myopathic syndrome (a rare disease requiring complex diagnosis). However, the cost of this analysis is very high, and mom will not be able to pay for it without your help. Let's support Aljanat and help her pass a genetic analysis, which will open up new horizons in understanding her health and give hope for an improved quality of life!