MUCOPOLYSACCHARIDOSIS (MPS) TYPE VI (MAROTEAUX LAMY), QUANTITATIVE, BLOOD
Maroteaux-Lamy is Type VI MPS due to deficient enzyme activity of Arylsulphatase B. It shows an autosomal recessive inheritance & onset is late infantile. Dermatan sulphate is excreted in urine. Patients present with hepatosplenomegaly, skeletal dysplasia, corneal clouding, coarse facies & valvular heart disease. An important hematologic finding is granulated neutrophils & lymphocytes. No cognitive degeneration is present.
Parameter(s) covered : 2
Report Frequency: Sample Daily by 4 pm; Report 4 days
Special Instruction: Provide brief clinical history.
Price : ₹ 1800.00
Parameters
- Control Value
- Patient Value