SMPD1
Acid Sphingomyelinase Deficiency (ASMD): SMPD1 Sequencing
Key Information
Lab:
TAT:
21 days
Price:
$800
CPT Code(s):
81479
Test Code:
DSMP
Prenatal Samples Accepted
Acid Sphingomyelinase Deficiency (ASMD): SMPD1 Sequencing
SMPD1 sequencing is a molecular test used to identify variants in the gene associated with acid sphingomyelinase deficiency, also known as Niemann-Pick A/B disease). This test can also confirm a diagnosis and identify disease-causing variants within a family to facilitate carrier screening.
Acid sphingomyelinase deficiency
Clinical Information
Acid sphingomyelinase deficiency (ASMD) includes three clinical phenotypes: Niemann-Pick disease type A, type B, and type A/B. Type A typically presents in early childhood with hepatosplenomegaly, failure to thrive, a cherry-red macular spot, pulmonary infiltration, and progressive neurologic degeneration. Type B presents later in life with hepatosplenomegaly and pulmonary infiltration, but with mild or absent neurologic involvement. Type A/B has similar organ involvement to type B, but symptoms may not appear until adulthood. Foam cells can be observed in the bone marrow of patients across all subtypes.
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 SMPD1 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
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
