GM1 GANGLIOSIDOSIS, QUANTITATIVE,BLOOD
GM1 gangliosidosis is an autosomal recesssive disorder due to deficiency of beta-galactosidase which leads to deposition of GM1 ganglioside, glycoproteins and keratin sulphate in brain and body organs.
Parameter(s) covered : 2
Report Frequency: Sample Daily by 4 pm; Report 4 days
Special Instruction: Provide brief clinical history.
Price : ₹ 1900.00
Parameters
- Control Value
- Patient Value