This test is only orderable by MCHS Wisconsin sites. This test is performed by the Wisconsin State Laboratory of Hygiene.
When this test is ordered the LDALD / Lysosomal and Peroxisomal Disorders Newborn Screen, Blood Spot and SMNDX / Spinal Muscular Atrophy Diagnostic Assay, Deletion/Duplication Analysis, Varies are automatically added. This test is collected on the Wisconsin State Laboratory of Hygiene collection card and the LDALD / Lysosomal and Peroxisomal Disorders Newborn Screen, Blood Spot and SMNDX / Spinal Muscular Atrophy Diagnostic Assay, Deletion/Duplication Analysis, Varies are collected on the Mayo Clinic Laboratories blood spot card. The LDALD test is performed by the Biochemical Genetics Laboratory and reported separately from WINS. The SMNDX test is performed by the Genomics Laboratory Molecular and also reported separately from WINS. The Biochemical Genetics Laboratory is responsible for ensuring tests are completed on babies born at Mayo Clinic Health Systems Wisconsin sites and for transcribing test results into the SOFT computer system.
For information on LDALD / Lysosomal and Peroxisomal Disorders Newborn Screen, Blood Spot and SMNDX / Spinal Muscular Atrophy Diagnostic Assay, Deletion/Duplication Analysis, Varies, see the individual Test IDs.
Blood spots
Newborn Screen
Newborn Screening
This test is only orderable by MCHS Wisconsin sites. This test is performed by the Wisconsin State Laboratory of Hygiene.
When this test is ordered the LDALD / Lysosomal and Peroxisomal Disorders Newborn Screen, Blood Spot and SMNDX / Spinal Muscular Atrophy Diagnostic Assay, Deletion/Duplication Analysis, Varies are automatically added. This test is collected on the Wisconsin State Laboratory of Hygiene collection card and the LDALD / Lysosomal and Peroxisomal Disorders Newborn Screen, Blood Spot and SMNDX / Spinal Muscular Atrophy Diagnostic Assay, Deletion/Duplication Analysis, Varies are collected on the Mayo Clinic Laboratories blood spot card. The LDALD test is performed by the Biochemical Genetics Laboratory and reported separately from WINS. The SMNDX test is performed by the Genomics Laboratory Molecular and also reported separately from WINS. The Biochemical Genetics Laboratory is responsible for ensuring tests are completed on babies born at Mayo Clinic Health Systems Wisconsin sites and for transcribing test results into the SOFT computer system.
For information on LDALD / Lysosomal and Peroxisomal Disorders Newborn Screen, Blood Spot and SMNDX / Spinal Muscular Atrophy Diagnostic Assay, Deletion/Duplication Analysis, Varies, see the individual Test IDs.
Whole blood
WINS: 4 blood spots
LDALD: 1 blood spot
Blood spot; Shows serum rings; Insufficient specimen | Reject |
Specimen Type | Temperature | Time | Special Container |
---|---|---|---|
Whole blood | Ambient (preferred) | 365 days | |
Frozen | 365 days | ||
Refrigerated | 365 days |
This test is only orderable by MCHS Wisconsin sites. This test is performed by the Wisconsin State Laboratory of Hygiene.
When this test is ordered the LDALD / Lysosomal and Peroxisomal Disorders Newborn Screen, Blood Spot and SMNDX / Spinal Muscular Atrophy Diagnostic Assay, Deletion/Duplication Analysis, Varies are automatically added. This test is collected on the Wisconsin State Laboratory of Hygiene collection card and the LDALD / Lysosomal and Peroxisomal Disorders Newborn Screen, Blood Spot and SMNDX / Spinal Muscular Atrophy Diagnostic Assay, Deletion/Duplication Analysis, Varies are collected on the Mayo Clinic Laboratories blood spot card. The LDALD test is performed by the Biochemical Genetics Laboratory and reported separately from WINS. The SMNDX test is performed by the Genomics Laboratory Molecular and also reported separately from WINS. The Biochemical Genetics Laboratory is responsible for ensuring tests are completed on babies born at Mayo Clinic Health Systems Wisconsin sites and for transcribing test results into the SOFT computer system.
For information on LDALD / Lysosomal and Peroxisomal Disorders Newborn Screen, Blood Spot and SMNDX / Spinal Muscular Atrophy Diagnostic Assay, Deletion/Duplication Analysis, Varies, see the individual Test IDs.
Monday through Friday
Not Applicable
S3620
Test Id | Test Order Name | Order LOINC Value |
---|---|---|
WINS | Wisconsin Newborn Screen | 54089-8 |
Result Id | Test Result Name |
Result LOINC Value
Applies only to results expressed in units of measure originally reported by the performing laboratory. These values do not apply to results that are converted to other units of measure.
|
---|---|---|
113124 | Wisconsin Newborn Screen | No LOINC Needed |
55323 | PHENYLKETONURIA: Phenylalanine | 29571-7 |
55324 | MAPLE SYRUP URINE DISEASE: Leucine | 38479-2 |
55325 | HOMOCYSTINURIA: Methionine | 63380-0 |
55326 | CITRULLINEMIA/ASA: Citrulline | 46733-2 |
55327 | TYROSINEMIA Type I: Succinylacetone | 46733-2 |
55328 | TYROSINEMIA Type II and III: Tyrosine | 46733-2 |
55329 | HYPOTHYROIDISM: TSH | 46762-1 |
55330 | ADRENAL HYPERPLASIA: 17-OHP | 46758-9 |
55331 | CYSTIC FIBROSIS: Trypsinogen | 46769-6 |
55332 | HEMOGLOBINOPATHIES: Hgb Pattern | 46740-7 |
55333 | FATTY ACID OXIDATION: Acylcarnitine Prof | 58088-6 |
55334 | ORGANIC ACIDEMIAS: Acylcarnitine Profile | 46733-2 |
55335 | GALACTOSEMIA: GALT Activity | 46737-3 |
55336 | BIOTINIDASE DEF: Biotinidase Activity | 46761-3 |
55337 | SCID-IMMUNODEFICIENCY: TREC | 62321-5 |
606121 | SPINAL MUSCULAR ATROPHY: SMN1 | 92004-1 |