A very rare cause of intestinal pseudoobstruction: familial visceral myopathy type IV
A very rare cause of intestinal pseudoobstruction: familial visceral myopathy type IV
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DOI：
10.1080/080352500750044115
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发表时间：
2000-06-01
期刊：
影响因子：
3.8
通讯作者：
Girgin, N
中科院分区：
文献类型：
--
作者：
Kansu, A;Ensari, A;Girgin, N
一种非常罕见的假性肠梗阻病因：家族性内脏肌病IV型。骨髓移植可能提供一种更确定的治疗方法的前景（个人通讯）。通过TNSALP基因的失活已经建立了婴儿低磷酸酶症的敲除小鼠模型（13），这为进一步了解该疾病和可能的基因治疗带来了希望。
A very rare cause of intestinal pseudoobstruction: familial visceral myopathy type IV alization in this condition. Bone marrow transplantation may offer the prospect of a more definitive treatment (pers. comm.). A knockout mouse model of infantile hypophosphatasia has been established by inactivation of the TNSALP gene (13) and this holds promise for further understanding of the disease and possibly for gene therapy.