Kamran was born healthy, but from his first years of life, it became clear that he was developing more slowly than his peers. Numerous examinations revealed serious disabilities: brain damage, static-motor developmental delay syndrome, and, finally, an unclassified genetic disorder with severe delayed psychomotor development. Kamran is unable to care for himself, shows no interest in toys, and does not play with other children.
Kamran has decreased muscle tone in his arms and increased mobility in his elbows. He has impaired muscle tone in his legs, with elements of spasticity. He has poor speech understanding, maintains brief eye contact, his attention is erratic, and he has difficulty sitting still.
Kamran was regularly monitored by a neurologist and epileptologist and received the necessary treatment, but his developmental delay persisted. In 2017, a rehabilitation course was completed, after which the boy regressed.
To help doctors develop an effective treatment plan for Kamran and support his development, a genetic study—complete genome sequencing—is necessary. This will help understand the cause of his condition and identify the most appropriate treatment options. Please donate to help Kamran.
