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HelpTest Code UNIPD Uniparental Disomy, Varies
Reporting Name
Uniparental DisomyPerforming Laboratory
Mayo Clinic Laboratories in Rochester
Useful For
Evaluation of patients presenting with mosaicism, confined placental mosaicism, or Robertsonian translocations
Evaluation of patients presenting with features of disorders known to be associated with uniparental disomy (eg, Russell-Silver syndrome)
Evaluation of disease mechanism in individuals with rare autosomal recessive disease and only one carrier parent
Method Name
Polymerase Chain Reaction (PCR)/Microsatellite markers
Ordering Guidance
This test is only intended to rule out whole-chromosome uniparental disomy (UPD). If testing is desired to rule out UPD 11 for Beckwith-Wiedemann syndrome or Russell-Silver syndrome, the recommended test is BWRS / Beckwith-Wiedemann Syndrome/Russell-Silver Syndrome, Molecular Analysis, Varies, as it will also detect cases caused by segmental UPD.
Shipping Instructions
Specimen preferred to arrive within 96 hours of collection.
Specimen Required
Specimens from both parents and the child or fetus are recommended for optimal interpretation of results. Each specimen must have a separate order for this test. Only the proband specimen will be charged.
Testing can be performed if only one parent specimen is submitted, however, biparental inheritance and some types of uniparental disomy (UPD) cannot be definitively established in the absence of one parent. Additionally, there is a higher likelihood for uninformative or inconclusive results.
If all required specimens are not received within one month of ordering, testing will be canceled.
Patient Preparation: A previous bone marrow transplant from an allogenic donor will interfere with testing. For instructions for testing patients who have received a bone marrow transplant, call 800-533-1710.
Submit only 1 of the following specimens:
Specimen Type: Whole blood
Preferred: Lavender top (EDTA) or yellow top (ACD)
Acceptable: Any anticoagulant
Specimen Volume: 3 mL
Collection Instructions:
1. Invert several times to mix blood.
2. Send whole blood specimen in original tube. Do not aliquot.
Specimen Stability Information: Ambient (preferred) 4 days/Refrigerated
Prenatal Specimens
Due to its complexity, consultation with the laboratory is required for all prenatal testing; call 800-533-1710 to speak to a genetic counselor.
Specimen Type: Amniotic fluid
Container/Tube: Amniotic fluid container
Specimen Volume: 20 mL
Specimen Stability Information: Refrigerated (preferred)/Ambient
Additional information: If amniotic fluid or culture amniotic fluid is received, CULAF / Culture for Genetic Testing, Amniotic Fluid will be added at an additional charge.
Specimen Type: Chorionic villi (CVS)
Container/Tube: 15-mL tube containing 15 mL of transport media
Specimen Volume: 20 mg
Specimen Stability Information: Refrigerated
Additional Information: If CVS or cultured CVS is received, CULFB / Fibroblast Culture for Biochemical or Molecular Testing will be added at an additional charge.
Acceptable:
Specimen Type: Confluent cultured cells
Container/Tube: T-25 flask
Specimen Volume: 2 Flasks
Collection Instructions: Submit confluent cultured cells from another laboratory.
Specimen Stability Information: Ambient (preferred)/Refrigerated (<24 hours)
Specimen Type
VariesSpecimen Minimum Volume
Blood: 0.5 mL
Amniotic Fluid: 10 mL
Chorionic Villi: 5 mg
Specimen Stability Information
| Specimen Type | Temperature | Time |
|---|---|---|
| Varies | Varies | |
Reject Due To
All specimens will be evaluated at Mayo Clinic Laboratories for test suitability.Reference Values
An interpretive report will be provided.
Interpretation
Microsatellite markers are compared between the proband and parental samples for the chromosome of interest. The pattern of the microsatellite markers will be classified as demonstrating uniparental disomy or biparental inheritance when sufficient informative markers are identified.
Day(s) Performed
Monday and Wednesday
Report Available
5 to 21 daysTest Classification
This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. It has not been cleared or approved by the US Food and Drug Administration.CPT Code Information
81402 – proband
81402 (if appropriate for parental specimen)
LOINC Code Information
| Test ID | Test Order Name | Order LOINC Value |
|---|---|---|
| UNIPD | Uniparental Disomy | 36917-3 |
| Result ID | Test Result Name | Result LOINC Value |
|---|---|---|
| 53356 | Result Summary | 50397-9 |
| 53357 | Result | 36917-3 |
| 53358 | Interpretation | 69047-9 |
| 53359 | Reason for Referral | 42349-1 |
| 53360 | Specimen | 31208-2 |
| 53361 | Source | 31208-2 |
| 53362 | Method | 85069-3 |
| 53363 | Released By | 18771-6 |
Forms
1. New York Clients-Informed consent is required. Document on the request form or electronic order that a copy is on file. The following documents are available:
-Informed Consent for Genetic Testing (T576)
-Informed Consent for Genetic Testing-Spanish (T826)
2. Molecular Genetics: Uniparental Disomy Patient Information
Reflex Tests
| Test ID | Reporting Name | Available Separately | Always Performed |
|---|---|---|---|
| CULFB | Fibroblast Culture for Genetic Test | Yes | No |
| CULAF | Amniotic Fluid Culture/Genetic Test | Yes | No |
Testing Algorithm
Polymerase chain reaction amplification of microsatellite markers on the chromosome of interest are used to test DNA from the parents and the child for the presence of uniparental disomy.
For prenatal specimens only:
If an amniotic fluid specimen or cultured amniocytes is received, amniotic fluid culture for genetic testing will be performed at an additional charge.
If a chorionic villus specimen or cultured chorionic villi is received, fibroblast culture for a genetic test will be performed at an additional charge.
For more information see:
-Prader-Willi and Angelman Syndromes: Laboratory Approach to Diagnosis
-Beckwith-Wiedemann and Russell-Silver Syndromes: Laboratory Approach to Diagnosis