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

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.

肝硬化患规检测避免漏诊。

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.

半症是另一种罕见的代谢功能紊乱疾病，因为缺乏分解半的酶（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A或其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（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紊乱疾病，因分解半乳糖的酶（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.

血症是另一种罕见的代谢功能紊乱疾病，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糖诊。

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。