{"id":12148,"date":"2025-03-13T20:22:43","date_gmt":"2025-03-13T19:22:43","guid":{"rendered":"https:\/\/valintermed.com\/?p=12148"},"modified":"2025-03-13T20:22:43","modified_gmt":"2025-03-13T19:22:43","slug":"sindrom-leya-unasledovannyy-po-materinskoy-linii","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/maternal-line-syndrome\/","title":{"rendered":"Leigh syndrome, inherited maternally"},"content":{"rendered":"
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Maternally inherited Leigh syndrome is a rare genetic disorder that typically manifests in young children. The disorder involves abnormal mitochondrial function, resulting in decreased energy production in cells. Leigh syndrome is characterized by progressive neurological decline, which can include symptoms such as muscle weakness, loss of coordination, hearing and vision impairment, and the development of psychomotor delay. The disorder is most often caused by mutations in mitochondrial genes that are inherited exclusively through the maternal line, making its presentation particularly relevant in the context of genetic predisposition and family history of the disorder.<\/p>\n

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