acanthocytosis symptoms
棘足细胞病症状
diagnosed with acanthocytosis
被诊断出患有棘足细胞病
severe acanthocytosis
重度棘足细胞病
treat acanthocytosis
治疗棘足细胞病
acanthocytosis causes
棘足细胞病病因
patient with acanthocytosis
患有棘足细胞病的患者
acanthocytosis test
棘足细胞病检测
neuroacanthocytosis syndrome
神经棘足细胞病综合征
hereditary acanthocytosis
遗传性棘足细胞病
acanthocytosis diagnosis
棘足细胞病诊断
acanthocytosis is characterized by the presence of spiky red blood cells in peripheral blood smears.
棘足细胞增多症的特征是在外周血涂片中存在带棘状的红细胞。
the patient presented with acanthocytosis and severe hemolytic anemia.
患者表现为棘足细胞增多症和严重的溶血性贫血。
laboratory analysis confirmed acanthocytosis associated with liver disease.
实验室分析证实了与肝病相关的棘足细胞增多症。
acanthocytosis can be inherited or acquired depending on the underlying condition.
棘足细胞增多症可能是遗传性或获得性，取决于潜在的病况。
blood smear examination revealed prominent acanthocytosis in the affected individual.
血涂片检查显示受影响的个体存在明显的棘足细胞增多症。
acanthocytosis is a key diagnostic feature of abetalipoproteinemia.
棘足细胞增多症是无β-脂蛋白血症的关键诊断特征。
the degree of acanthocytosis correlated with disease severity in the study.
该研究表明，棘足细胞增多症的程度与疾病的严重程度相关。
treatment for acanthocytosis focuses on managing the underlying cause.
治疗棘足细胞增多症的重点是管理潜在的原因。
genetic testing revealed mutations linked to hereditary acanthocytosis.
遗传检测显示了与遗传性棘足细胞增多症相关的突变。
acanthocytosis may be transient or permanent depending on etiology.
棘足细胞增多症可能是短暂的或永久的，取决于病因。
the mechanism of acanthocytosis involves lipid membrane abnormalities.
棘足细胞增多症的机制涉及脂质膜异常。
peripheral blood smear showed significant acanthocytosis alongside other abnormal findings.
外周血涂片显示，伴有其他异常发现，存在明显的棘足细胞增多症。
acanthocytosis symptoms
棘足细胞病症状
diagnosed with acanthocytosis
被诊断出患有棘足细胞病
severe acanthocytosis
重度棘足细胞病
treat acanthocytosis
治疗棘足细胞病
acanthocytosis causes
棘足细胞病病因
patient with acanthocytosis
患有棘足细胞病的患者
acanthocytosis test
棘足细胞病检测
neuroacanthocytosis syndrome
神经棘足细胞病综合征
hereditary acanthocytosis
遗传性棘足细胞病
acanthocytosis diagnosis
棘足细胞病诊断
acanthocytosis is characterized by the presence of spiky red blood cells in peripheral blood smears.
棘足细胞增多症的特征是在外周血涂片中存在带棘状的红细胞。
the patient presented with acanthocytosis and severe hemolytic anemia.
患者表现为棘足细胞增多症和严重的溶血性贫血。
laboratory analysis confirmed acanthocytosis associated with liver disease.
实验室分析证实了与肝病相关的棘足细胞增多症。
acanthocytosis can be inherited or acquired depending on the underlying condition.
棘足细胞增多症可能是遗传性或获得性，取决于潜在的病况。
blood smear examination revealed prominent acanthocytosis in the affected individual.
血涂片检查显示受影响的个体存在明显的棘足细胞增多症。
acanthocytosis is a key diagnostic feature of abetalipoproteinemia.
棘足细胞增多症是无β-脂蛋白血症的关键诊断特征。
the degree of acanthocytosis correlated with disease severity in the study.
该研究表明，棘足细胞增多症的程度与疾病的严重程度相关。
treatment for acanthocytosis focuses on managing the underlying cause.
治疗棘足细胞增多症的重点是管理潜在的原因。
genetic testing revealed mutations linked to hereditary acanthocytosis.
遗传检测显示了与遗传性棘足细胞增多症相关的突变。
acanthocytosis may be transient or permanent depending on etiology.
棘足细胞增多症可能是短暂的或永久的，取决于病因。
the mechanism of acanthocytosis involves lipid membrane abnormalities.
棘足细胞增多症的机制涉及脂质膜异常。
peripheral blood smear showed significant acanthocytosis alongside other abnormal findings.
外周血涂片显示，伴有其他异常发现，存在明显的棘足细胞增多症。
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