20 Hrs
Source:
الشرق
Child's treatment at Siddra leads to discovery
The article highlighted the story of a child who suffered from recurrent infections and digestive problems, which led to the discovery of a previously unidentified genetic mutation. His condition was diagnosed after conducting genetic tests that revealed a low level of a crucial protein responsible for immune cell functions, resulting in immobility of his immune cells. Using a medication that stimulated the restoration of his immune cells to their normal state, his condition significantly improved, reflecting a development in the concept of "precision medicine" that focuses on directly treating the specific cause of the disease.
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