stomatocytosis वाक्य
उदाहरण वाक्य
मोबाइल
- Stomatocytosis is also found as a hereditary disease in Alaskan malamute and miniature schnauzer dogs.
- Stomatin is a 31 kDa integral membrane protein, named after the rare human haemolytic anaemia hereditary stomatocytosis.
- Loss of localization of the encoded protein is associated with hereditary stomatocytosis, a form of hemolytic anemia.
- The two varieties of stomatocytosis classified with respect to hydration status are overhydrated ( hydrocytosis ) and dehydrated ( xerocytosis ).
- Piezo1 is also found in red blood cells, and gain of function mutations in the channels are associated with hereditary xerocytosis or stomatocytosis.
- Disorders of the proteins in these membranes are associated with many disorders, such as hereditary spherocytosis, hereditary elliptocytosis, hereditary stomatocytosis, and paroxysmal nocturnal hemoglobinuria.
- More importantly erythroid AE1 mutations cause 15 25 % of cases of Hereditary spherocytosis ( a disorder associated with progressive red cell membrane loss ), and also cause the hereditary conditions of Hereditary stomatocytosis and Southeast Asian Ovalocytosis
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