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[肠道源性家族性高磷酸酶血症]

[Familial hyperphosphatasemia of intestinal origin].

作者信息

Carrascosa C, Parra S, Lorenzo I, Marín C, Miras M, de la Peña C, Martínez P

机构信息

Servicio de Análisis Clínicos, Hospital Universitario Virgen de la Arrixaca, El Palmar, Murcia.

出版信息

Rev Esp Enferm Dig. 1995 Apr;87(4):327-9.

PMID:7794642
Abstract

To clarify the diagnostic laboratory procedures before a case of unknown origin hyperphosphatasemia, we have studied the electrophoretic separation of serum alkaline phosphatase activity on agarose gel with and without neuraminidase. Sera were collected from a family, four of whom showed hyperphosphatasemia. Alkaline phosphatase isoenzyme patterns on agarose gel electrophoresis demonstrated that two persons out of the six members tested had unusual isozymes, the hydrophilic and the hydrophobic intestinal isozyme representing more than 50% of total alkaline phosphatase. The advantages of this method are its simplicity and low cost. The early recognition of this benign abnormality should help to avoid unnecessary diagnostic tests (i.e. image or radioisotopic examination).

摘要

为了明确不明原因高磷酸酶血症病例的诊断实验室程序,我们研究了在有无神经氨酸酶的情况下,血清碱性磷酸酶活性在琼脂糖凝胶上的电泳分离。从一个家族中采集血清,该家族中有四人表现出高磷酸酶血症。琼脂糖凝胶电泳上的碱性磷酸酶同工酶图谱显示,在测试的六名成员中,有两人具有异常同工酶,亲水性和疏水性肠同工酶占总碱性磷酸酶的50%以上。该方法的优点是简单且成本低。早期识别这种良性异常有助于避免不必要的诊断检查(即影像学或放射性同位素检查)。

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