{"id":12174,"date":"2025-01-14T19:21:45","date_gmt":"2025-01-14T18:21:45","guid":{"rendered":"https:\/\/valintermed.com\/?p=12174"},"modified":"2025-01-14T19:21:45","modified_gmt":"2025-01-14T18:21:45","slug":"sindrom-mune-kuna","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/i-have-a-cold-syndrome\/","title":{"rendered":"Mounier-Kuhn syndrome"},"content":{"rendered":"
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Mounier-Kuhn syndrome (spinal muscular atrophy type 2) is a rare genetic disorder characterized by progressive muscle weakness and dysfunction. The disorder is caused by degeneration of motor neurons in the spinal cord, resulting in decreased muscle tone and skeletal muscle atrophy, most commonly in the distal regions. Symptoms can range from mild to severe, sometimes appearing in early childhood and sometimes later in life. Clinical manifestations may include difficulty walking, decreased motor skills, and respiratory problems related to weakness of the respiratory muscles. <\/p>\n

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