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。

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，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辅A位或其辅腺苷钴胺素缺陷所致的一种遗传性代谢疾。

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疾，因为缺乏分解半乳糖的（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.

半乳症是另一种罕见的功能紊乱病，因为缺乏分解半乳的酶（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。

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

乳糖血症是另一种罕见的代谢功能紊乱，因为缺乏分解乳糖的酶（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血糖避免漏。

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

丙二酸血症是由于丙二酰辅酶A位酶或其辅酶腺苷钴胺素缺陷所致遗传性代谢疾病。

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

半乳糖血症是另罕见代谢功能紊乱疾病，因为缺乏分解半乳糖酶（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谢功能紊乱疾病，因为缺乏分解半乳糖的酶（高尔特？）所。