ARUP's Laboratory Test Directory

Vascular Malformations Sequencing, 10 Genes : 2007390
[ image for: Patient History for Vascular Malformation Syndrome Testing]
Patient History for Vascular Malformation Syndrome Testing
[ image for: Additional Technical Information]
Additional Technical Information


Mnemonic: VASC SEQ

Methodology: Massive Parallel Sequencing
Performed: Varies
Reported: Within 84 days
Specimen Required: Collect: Lavender (EDTA) or yellow (ACD Solution A or B).

Specimen Preparation: Transport 3 mL whole blood. (Min: 1 mL)

Storage/Transport Temperature: Refrigerated.

Remarks: Submit the Patient History Form for Vascular Malformations with the Electronic Packing List.

Stability (collection to initiation of testing): Ambient: 72 hours; Refrigerated: 1 week; Frozen: Unacceptable
Reference Interval:
By report
Interpretive Data: Refer to report.



Counseling and informed consent are recommended for genetic testing. Consent forms are available online at www.aruplab.com.

See Compliance Statement C: www.aruplab.com/CS
CPT Code(s): 81321 (PTEN); 81479
Cross References: 002470 PTEN-Related Disorders (PTEN) Sequencing and Deletion/Duplication , 0051348 Hereditary Hemorrhagic Telangiectasia (ACVRL1 and ENG) Deletion/Duplication , 0051382 Hereditary Hemorrhagic Telangiectasia (ACVRL1 and ENG) Sequencing and Deletion Duplication , 0051510 Juvenile Polyposis (SMAD4) Sequencing , 0051575 Hereditary Hemorrhagic Telangiectasia (ACVRL1 and ENG) Sequencing , 0051789 Juvenile Polyposis (SMAD4) Sequencing and Deletion/Duplication , 2001976 Juvenile Polyposis (SMAD4) Deletion/Duplication , 2002722 PTEN-Related Disorders (PTEN) Sequencing , 2002726 PTEN-Related Disorders (PTEN) Deletion/Duplication , 2002730 RASA1-Related Disorders (RASA1) Sequencing , 2003152 Cerebral Cavernous Malformation (CCM1) Sequencing , 2003156 Cerebral Cavernous Malformation (CCM2) Sequencing , 2003160 Cerebral Cavernous Malformation (CCM3) Sequencing , 2003164 Cerebral Cavernous Malformation (CCM1) Sequencing with Reflex to (CCM1, CCM2 and CCM3) Delet , 2003172 Cerebral Cavernous Malformation (CCM1, CCM2, and CCM3) Deletion/Duplication