Conclusion Saccharic metabolic disorder occurred easily in patient with hepatic cirrhosis，eventually develope into diabetes.

肝硬化患者应常规检测血糖避免漏诊。

Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.

甲基丙二酸血症是由于甲基丙二酰辅酶A位酶或其辅酶腺苷钴胺素缺陷所致的一种遗传性代谢疾病。

Galactosemia is another rare metabolic disorder that occurs when the liver enzyme GALT, needed to break down galactose, is partially or completely absent.

半乳糖血症是另一种罕见的代谢功能紊乱疾病，因为缺乏分解半乳糖的酶（高尔特？）所致。

Conclusion Saccharic metabolic disorder occurred easily in patient with hepatic cirrhosis，eventually develope into diabetes.

肝硬化患者应常规检测糖避免漏诊。

Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.

甲基丙二是由于甲基丙二酰辅酶A位酶或其辅酶腺苷钴胺所致的一种遗传性代谢疾病。

Galactosemia is another rare metabolic disorder that occurs when the liver enzyme GALT, needed to break down galactose, is partially or completely absent.

半乳糖是另一种罕见的代谢功能紊乱疾病，因为乏分解半乳糖的酶（高尔特？）所致。

Conclusion Saccharic metabolic disorder occurred easily in patient with hepatic cirrhosis，eventually develope into diabetes.

肝硬化患者应常规检测糖避免漏诊。

Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.

甲基丙二酸由于甲基丙二酰辅酶A位酶或其辅酶腺苷钴陷所致的一种遗传性代谢疾病。

Galactosemia is another rare metabolic disorder that occurs when the liver enzyme GALT, needed to break down galactose, is partially or completely absent.

半乳糖另一种罕见的代谢功能紊乱疾病，因为乏分解半乳糖的酶（高尔特？）所致。

Conclusion Saccharic metabolic disorder occurred easily in patient with hepatic cirrhosis，eventually develope into diabetes.

肝硬化患者应常规检测血糖避免漏诊。

Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.

甲基丙二酸血症是由于甲基丙二酰辅酶A位酶或其辅酶腺苷钴胺素缺陷所致的一种遗传性代谢疾病。

Galactosemia is another rare metabolic disorder that occurs when the liver enzyme GALT, needed to break down galactose, is partially or completely absent.

半乳糖血症是另一种罕见的代谢功能紊乱疾病，因为缺乏分解半乳糖的酶（高尔特？）所致。

Conclusion Saccharic metabolic disorder occurred easily in patient with hepatic cirrhosis，eventually develope into diabetes.

肝硬化患者应常规检测血避免漏诊。

Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.

甲基丙二酸血症是由于甲基丙二酰辅酶A位酶或其辅酶腺苷钴胺素缺陷所致一种遗传性代谢疾病。

Galactosemia is another rare metabolic disorder that occurs when the liver enzyme GALT, needed to break down galactose, is partially or completely absent.

半血症是另一种罕见代谢功能紊乱疾病，因为缺乏分解半酶（高尔特？）所致。

Conclusion Saccharic metabolic disorder occurred easily in patient with hepatic cirrhosis，eventually develope into diabetes.

肝硬化患者应常规检测血糖避免漏诊。

Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.

甲基丙二酸血症甲基丙二酰辅酶A位酶或其辅酶腺素缺陷所致的一种遗传性代谢疾病。

Galactosemia is another rare metabolic disorder that occurs when the liver enzyme GALT, needed to break down galactose, is partially or completely absent.

半乳糖血症另一种罕见的代谢功能紊乱疾病，因为缺乏分解半乳糖的酶（高尔特？）所致。

Conclusion Saccharic metabolic disorder occurred easily in patient with hepatic cirrhosis，eventually develope into diabetes.

肝硬化患者应常规检测血糖避免漏诊。

Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.

甲基丙二酸血症是由于甲基丙二酰辅酶A位酶或其辅酶腺苷钴胺素缺陷所的一种遗传性代谢疾病。

Galactosemia is another rare metabolic disorder that occurs when the liver enzyme GALT, needed to break down galactose, is partially or completely absent.

半乳糖血症是另一种罕见的代谢功能紊乱疾病，因为缺乏分解半乳糖的酶（高尔特？）所。

Conclusion Saccharic metabolic disorder occurred easily in patient with hepatic cirrhosis，eventually develope into diabetes.

肝硬化患者应常规检测血避免漏诊。

Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.

甲基丙二酸血症是由于甲基丙二酰辅酶A位酶或其辅酶腺苷钴胺素缺陷所致的一种遗传性谢疾病。

Galactosemia is another rare metabolic disorder that occurs when the liver enzyme GALT, needed to break down galactose, is partially or completely absent.

血症是另一种罕见的谢功能紊乱疾病，因为缺乏分解的酶（高尔特？）所致。

Conclusion Saccharic metabolic disorder occurred easily in patient with hepatic cirrhosis，eventually develope into diabetes.

肝硬化患者应常规检测血糖避免漏诊。

Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.

甲基丙二酸血症是由于甲基丙二酰辅酶A位酶或其辅酶腺苷钴胺素缺陷所的一种遗传性疾病。

Galactosemia is another rare metabolic disorder that occurs when the liver enzyme GALT, needed to break down galactose, is partially or completely absent.

半乳糖血症是另一种罕见的功能紊乱疾病，因为缺乏分解半乳糖的酶（高尔？）所。

Conclusion Saccharic metabolic disorder occurred easily in patient with hepatic cirrhosis，eventually develope into diabetes.

肝硬化患者应常规检测血糖避免漏诊。

Methylmalonic acidemia is an inherited metabolic disorder,which is caused by deficiency of methylmalonyl-coenzyme A mutase or its cofactor adenosylcobalamin.

甲基丙二酸血症是由于甲基丙二酰辅酶A位酶或其辅酶腺苷钴胺素缺陷所致的一种遗传性代谢病。

Galactosemia is another rare metabolic disorder that occurs when the liver enzyme GALT, needed to break down galactose, is partially or completely absent.

半乳糖血症是另一种罕见的代谢功能病，因为缺乏分解半乳糖的酶（高尔特？）所致。