{"id":12109,"date":"2025-03-13T21:43:20","date_gmt":"2025-03-13T20:43:20","guid":{"rendered":"https:\/\/valintermed.com\/?p=12109"},"modified":"2025-03-13T21:43:20","modified_gmt":"2025-03-13T20:43:20","slug":"monomelicheskaya-amiotrofiya","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/monomelicheskaia-amyotrophia\/","title":{"rendered":"Monomelic amyotrophy"},"content":{"rendered":"
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Monomelic amyotrophy, also known as Benedict's syndrome, is a rare neurological disorder characterized by progressive muscle wasting, usually in one limb. It is a motor neuron disorder characterized by isolated muscle weakness due to degeneration of the anterior ronary neurons that supply the muscles. Monomelic amyotrophy typically begins with weakness of the shoulder or leg muscles, which in later stages leads to significant atrophy. Clinical manifestations may vary, but the main symptom is asymmetric weakness, which may progress to more severe forms of motor impairment. The disorder typically affects adults and is most often seen in men, highlighting the importance of studying the etiology and pathogenesis of the disease.<\/p>\n

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