Abstract:Introduction: Rare diseases are those which occur in 1 person in 2000. Usually they are genetically conditioned. They also comprise diseases which appear as a result of metabolic, immunological defects, infections and uncommon cancers. Development of science, especially genetics prompted discovery of new gene’s mutations. One of them is a mutation of ATP1A3 which alternating hemiplegia of childhood. It is a disease whose manifestations appear in early childhood and are unpredictable. Strokes can be hemiplegic … Show more
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