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遗传性球形红细胞增多症的特点是球形红细胞及网织红细胞增多,红细胞脆性增高,有不同程度的贫血,黄疸和肝脾肿大。临床上容易误诊为黄疸型肝炎。现将我院收治3例报告如下。临床资料3例中男性2例,女性1例。发病年龄:2岁
Hereditary spherocytosis is characterized by spherical red blood cells and reticulocytes increased erythrocyte fragility increased with varying degrees of anemia, jaundice and hepatosplenomegaly. Clinically easy to misdiagnosed as jaundice hepatitis. Now in our hospital admitted 3 cases are as follows. Three cases of clinical data in 2 males and 1 females. Age of onset: 2 years old