Congenital disorder of glycosylation caused by mutation of ATP6AP1 gene (c.1036G>A) in a Chinese infant: A case report

Table 2 Results of several follow-up examinations and medications for the child

Age	ALT	AST	IgG	IgA	IgM	Blood ammonia	Medication
8 mo	213	242	4.2	1.3	0.54	181	Glutathione, ursodeoxycholic acid, ornithine monohydrate
9 mo	202	332	3.5	0.1	0.16	74	Glutathione, ​compound glycyrrhizin
11 mo	388	515	-	-	-	-	Glutathione, ​compound glycyrrhizin
12 mo	167	111	3.12	0.37	0.36	142	Glutathione, ​compound glycyrrhizin, ornithine monohydrate
19 mo	128	196	2.16	0.32	0.09	95	Bicyclol, compound glycyrrhizin

ALT: Alanine aminotransferase; AST: Aspartate aminotransferase; Ig: Immunoglobulin.