{"id":12191,"date":"2025-01-14T18:42:00","date_gmt":"2025-01-14T17:42:00","guid":{"rendered":"https:\/\/valintermed.com\/?p=12191"},"modified":"2025-01-14T18:42:00","modified_gmt":"2025-01-14T17:42:00","slug":"sindrom-neyroakantotsitoza-makleoda","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/makleoda-neuroacanthositoza-syndrome\/","title":{"rendered":"McLeod neuroacanthocytosis syndrome"},"content":{"rendered":"
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McLeod neuroacanthocytosis syndrome is a rare hereditary neurological disorder characterized by specific changes in the brain and peripheral nervous system. It is manifested by a combination of movement disorders, a sullen state, coordination disorders, and multiple ulcers on the skin. One of the key features of the syndrome is the presence of acanthocytes - abnormal forms of red blood cells. This syndrome can also be accompanied by mental disorders, learning problems and disproportionate growth, which makes its clinical picture diverse. McLeod syndrome has a genetic nature and is predominantly inherited in an autosomal recessive manner, often occurring in males.<\/p>\n

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