Short link on March 10, 2025, 15:11 Dmitry Runkevich Researcher at the Department of Molecular Mechanisms of Hereditary Disorders of Metabolism of the MGNC named after N.P. Bochkova Julia Itkis spoke in a conversation with RT about the disease, from which the 22-year-old Prince of Luxembourg Frederick died. “Gene Polg is associated with hereditary diseases related to the group of primary mitochondrial pathologies,” the specialist explained the frequent of them: Alpers syndrome, Sando syndrome, syndrome syndrome Mitochondrial neurogastestinal encephalopathy, progressing external ophthalmoplegia, noted the geneticist. “At different stages, mitochondrial diseases from this group can occur under masks of other hereditary and acquired diseases, which complicates the diagnosis, especially in the early stages of the disease,” the expert noted, in these diseases, many systems and many systems are affected and many systems are affected and many systems are affected and many systems are affected Organs, including the brain, muscles and liver, and symptoms can be varied and very severe. In some forms of these diseases, stroke -like episodes and epileptic attacks often occur. “Today, methods for diagnosing mutations in the Polg gene, but pathogenetic therapy for this group of diseases, are not very well developed. The treatment is only symptomatic, ”the expert summed up. It became known that the 22-year-old Prince of Luxembourg Frederick died due to the rare genetic disease-mitochondrial illness associated with the mutations of the Polg. Highlight it and click “Ctrl + Enter” Subscribe to our channel in Zen
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