Medical Genetics Test Details
View Custom Req | Tests in Custom Req: 0
POLG - Related Disorders (POLG1, POLGA) tests available.
Alpers-Huttenlocher Syndrome | Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions Autosomal Dominant 1 | Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions Autosomal Recessive | Sensory Ataxic Neuropathy Dysarthria and Ophthalmoparesis | Juvenile Spinocerebellar Ataxia-Epilepsy Syndrome (SCAE) | ad-PEO | POLG - Related Sensory Ataxic Neuropathy Dysarthria and Ophthalmoparesis | MNGIE without Leukoencephalopathy
(Click the blue dot to view test details. Red dot = current test.)
Diagnostic Testing | Familial Mutation/Variant Analysis | Mutation Testing General Population | Prenatal Diagnosis | Presymptomatic Testing | |
---|---|---|---|---|---|
Deletion/Duplication Analysis |
![]() Test Code: 3068 |
||||
Sequence & Deletion/Duplication Analysis |
![]() Test Code: 3069 |
||||
Sequence Analysis |
![]() Test Code: 3065 |
![]() Test Code: 3066 This test can only be performed if there is a previously identified familial mutation. |
![]() Test Code: 60587 We require that the referring center consult with our laboratory genetic counselors regarding prenatal cases prior to submitting any samples. Please call 1-800-411-4363. ![]() Test Code: 3067 We require that the referring center consult with our laboratory genetic counselors regarding prenatal cases prior to submitting any samples. Please call 1-800-411-4363. |