acanthocytosis symptoms
棘紅細胞症的症狀
diagnosed with acanthocytosis
診斷為棘紅細胞症
severe acanthocytosis
嚴重的棘紅細胞症
treat acanthocytosis
治療棘紅細胞症
acanthocytosis causes
棘紅細胞症的病因
patient with acanthocytosis
患有棘紅細胞症的病人
acanthocytosis test
棘紅細胞症的檢查
neuroacanthocytosis syndrome
神經棘紅細胞症候群
hereditary acanthocytosis
遺傳性棘紅細胞症
acanthocytosis diagnosis
棘紅細胞症的診斷
acanthocytosis is characterized by the presence of spiky red blood cells in peripheral blood smears.
棘形紅血球症的特徵是在週邊血液抹片中出現棘形紅血球。
the patient presented with acanthocytosis and severe hemolytic anemia.
患者出現棘形紅血球症及嚴重溶血性貧血。
laboratory analysis confirmed acanthocytosis associated with liver disease.
實驗室分析確認棘形紅血球症與肝臟疾病有關。
acanthocytosis can be inherited or acquired depending on the underlying condition.
棘形紅血球症根據潛在病因可能是遺傳或後天獲得。
blood smear examination revealed prominent acanthocytosis in the affected individual.
血液抹片檢查顯示受影響個體有明顯的棘形紅血球症。
acanthocytosis is a key diagnostic feature of abetalipoproteinemia.
棘形紅血球症是無β脂蛋白血症的關鍵診斷特徵。
the degree of acanthocytosis correlated with disease severity in the study.
研究中棘形紅血球症的程度與疾病嚴重程度相關。
treatment for acanthocytosis focuses on managing the underlying cause.
棘形紅血球症的治療重點在於控制潛在病因。
genetic testing revealed mutations linked to hereditary acanthocytosis.
基因檢測顯示與遺傳性棘形紅血球症相關的突變。
acanthocytosis may be transient or permanent depending on etiology.
棘形紅血球症根據病因可能是暫時或永久的。
the mechanism of acanthocytosis involves lipid membrane abnormalities.
棘形紅血球症的機制涉及脂質膜異常。
peripheral blood smear showed significant acanthocytosis alongside other abnormal findings.
週邊血液抹片顯示有顯著的棘形紅血球症，並伴有其他異常發現。
acanthocytosis symptoms
棘紅細胞症的症狀
diagnosed with acanthocytosis
診斷為棘紅細胞症
severe acanthocytosis
嚴重的棘紅細胞症
treat acanthocytosis
治療棘紅細胞症
acanthocytosis causes
棘紅細胞症的病因
patient with acanthocytosis
患有棘紅細胞症的病人
acanthocytosis test
棘紅細胞症的檢查
neuroacanthocytosis syndrome
神經棘紅細胞症候群
hereditary acanthocytosis
遺傳性棘紅細胞症
acanthocytosis diagnosis
棘紅細胞症的診斷
acanthocytosis is characterized by the presence of spiky red blood cells in peripheral blood smears.
棘形紅血球症的特徵是在週邊血液抹片中出現棘形紅血球。
the patient presented with acanthocytosis and severe hemolytic anemia.
患者出現棘形紅血球症及嚴重溶血性貧血。
laboratory analysis confirmed acanthocytosis associated with liver disease.
實驗室分析確認棘形紅血球症與肝臟疾病有關。
acanthocytosis can be inherited or acquired depending on the underlying condition.
棘形紅血球症根據潛在病因可能是遺傳或後天獲得。
blood smear examination revealed prominent acanthocytosis in the affected individual.
血液抹片檢查顯示受影響個體有明顯的棘形紅血球症。
acanthocytosis is a key diagnostic feature of abetalipoproteinemia.
棘形紅血球症是無β脂蛋白血症的關鍵診斷特徵。
the degree of acanthocytosis correlated with disease severity in the study.
研究中棘形紅血球症的程度與疾病嚴重程度相關。
treatment for acanthocytosis focuses on managing the underlying cause.
棘形紅血球症的治療重點在於控制潛在病因。
genetic testing revealed mutations linked to hereditary acanthocytosis.
基因檢測顯示與遺傳性棘形紅血球症相關的突變。
acanthocytosis may be transient or permanent depending on etiology.
棘形紅血球症根據病因可能是暫時或永久的。
the mechanism of acanthocytosis involves lipid membrane abnormalities.
棘形紅血球症的機制涉及脂質膜異常。
peripheral blood smear showed significant acanthocytosis alongside other abnormal findings.
週邊血液抹片顯示有顯著的棘形紅血球症，並伴有其他異常發現。
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