α-N-acetylglucosaminidase

MPS IIIB

Chemical Pathology - Enzyme

For the diagnosis of MPS Type IIIB. The enzyme α-N-acetylglucosaminidase is deficient in leucocytes, plasma, and cultured cells in cases of Mucopolysaccharidosis Type IIIB

1. 5 - 10 mL lithium heparin whole blood or

2. Cultured fibroblasts or

3. Chorionic villi or

4. Cultured Chorionic villi or

5. Cultured amniotic cells

1. Send whole blood at ambient room temperature to reach the lab ideally within 24 hours of collection

2. Send flask completely filled with medium at room temperature a in well insulated container. To reach lab ideally within 24 hours

3. Contact the Enzyme Laboratory PRIOR to sampling and shipping

4. Contact the Enzyme Laboratory PRIOR to sampling and shipping

5. Contact the Enzyme Laboratory PRIOR to sampling and shipping

1. 4 to 6 weeks

2. 4 to 6 weeks

3. As soon as practically possible

4. As soon as practically possible

5. As soon as practically possible

Mucopolysaccharidosis Type IIIB, MPS Type IIIB, Sanfilippo B, Sanfilippo B syndrome, α-glucosaminidase

1. Yes

2. Yes

3. Yes

4. Yes

5. Yes