{"id":11607,"date":"2025-07-26T10:28:08","date_gmt":"2025-07-26T08:28:08","guid":{"rendered":"https:\/\/valintermed.com\/?p=11607"},"modified":"2025-07-26T10:28:08","modified_gmt":"2025-07-26T08:28:08","slug":"nasledstvennyy-ovalotsitoz","status":"publish","type":"post","link":"https:\/\/valintermed.com\/en\/medlibrary\/hereditary-ovalotsitosis\/","title":{"rendered":"Hereditary ovalocytosis"},"content":{"rendered":"
<\/div>\n

Hereditary ovalocytosis is a rare genetic disorder that belongs to the group of hereditary anemias, characterized by a change in the shape of red blood cells to ovaloid. This pathological condition leads to a decrease in the survival of red blood cells and their ability to effectively transport oxygen, which in turn causes chronic anemia. Cell shape abnormalities are usually concentrated in the peripheral blood, where the number of ovalocytes can significantly exceed normal values. The disease can occur with varying degrees of severity, ranging from asymptomatic to severe anemia, which requires specific treatment.<\/p>\n

\n
\n

Content<\/p>\nToggle<\/span><\/path><\/svg><\/svg><\/span><\/span><\/span><\/a><\/span><\/div>\n