ARSB
Maroteaux-Lamy Syndrome (MPS VI): ARSB Sequencing
Key Information
Lab:
TAT:
21 days
Price:
$800
CPT Code(s):
81479
Test Code:
DARB
Prenatal Samples Accepted
Maroteaux-Lamy Syndrome (MPS VI): ARSB Sequencing
ARSB sequencing is a molecular test used to identify variants in the gene associated with Maroteaux-Lamy syndrome (MPS VI). This test can also confirm a diagnosis and identify disease-causing variants within a family to facilitate carrier screening.
Maroteaux-Lamy syndrome (MPSVI)
Clinical Information
Maroteaux-Lamy syndrome (MPS VI) is a lysosomal storage disorder caused by a deficiency in the arylsulfatase B enzyme.The clinical features include short stature, corneal clouding, hepatosplenomegaly, cardiac abnormalities, and skeletal findings such as dysostosis multiplex and joint contractures. However, unlike many of the other MPS disorders, individuals with Maroteaux-Lamy generally have normal intelligence. Maroteaux Lamy syndrome is characterized by short stature, coarse facies, corneal clouding, joint stiffness and contractures and splenomegaly. Other features may include inguinal hernia, obstructive airway disease, skeletal abnormalities and cardiac valve disease. The progression of Maroteaux Lamy syndrome varies among affected individuals, and intelligence is typically not affected.
Technical Information
Specimen Requirements
Transport Instructions
Prenatal Testing Information
Prenatal diagnosis may be available for familial pathogenic or likely pathogenic variants; full sequencing of the ARSB gene is not available. For variants identified at external laboratories, GGC will need to review the variant classification prior to sample receipt.
Prenatal diagnosis is not available for variants of uncertain clinical significance. Additional fees for cell culture and maternal cell contamination may apply. Maternal cell contamination studies are required for all prenatal molecular tests. Contact the laboratory prior to sending a prenatal specimen to confirm that targeted testing can be accepted.
Prenatal Specimen Requirements
Prenatal Transport Instructions
Associated Tests
- Comprehensive Pulmonary NGS Panel
- Hermansky-Pudlak Syndrome & Pulmonary Fibrosis NGS Panel
- Maroteaux-Lamy Syndrome (MPS VI): Arylsulfatase B Enzyme Analysis
- Maroteaux-Lamy Syndrome (MPS VI): Urine Monitoring (Total GAGs, DS)
- Maternal Cell Contamination
- Mucopolysaccharidosis (MPS) Enzyme Panel
- Mucopolysaccharidosis (MPS) Enzyme Panel (DBS)
- Mucopolysaccharidosis (MPS) Urine Analysis (Total GAGs, DS, CS, KS, HS)
- Storage Disease Panel
- Targeted Analysis: Known Familial Variant
- Total Glycosaminoglycans (GAGs) Analysis
Connect With Our Experts
Call 1-800-473-9411 to speak with our team of laboratory genetic counselors for questions or additional information.
Robin Fletcher, MS, CGC
Falecia Thomas, MS, CGC
Alex Finley, MS, CGC
