Disease | Transport abnormality |
Sickle cell syndromes | Cellular dehydration mediated by increases in K-Cl cotransport and activity of the calcium-activated (Gardos) potassium channel |
Beta thalassemia | Relative cellular dehydration mediated by K-Cl cotransport |
Hemoglobin C disease | Cellular dehydration mediated by increased K-Cl cotransport |
Hereditary spherocytosis | Increased sodium and potassium permeability |
Hereditary stomatocytosis | Hyperhydration due to increased sodium permeability or dehydration (xerocytosis) associated with enhanced potassium loss |
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