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Test ID WINS Wisconsin Newborn Screen, Blood Spot

Testing Algorithm

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.

Reporting Name

Wisconsin Newborn Screen

Specimen Type

Whole blood

Specimen Minimum Volume

WINS: 4 blood spots
LDALD: 1 blood spot

Specimen Stability Information

Specimen Type Temperature Time Special Container
Whole blood Ambient (preferred) 365 days
  Frozen  365 days
  Refrigerated  365 days

CPT Code Information

S3620

LOINC Code Information

Test ID Test Order Name Order LOINC Value
WINS Wisconsin Newborn Screen 54089-8

 

Result ID Test Result Name Result LOINC Value
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

Day(s) Performed

Monday through Friday

Test Classification

Not Applicable