Frequently Asked Questions

1Do you accept insurance?
Medical consultations and genetic testing are self-pay only; no insurance is accepted currently. Testing cost is paid in addition to the consultation.
2How do I know if I need genetic testing?
During your consultation with Dr. Paul, he will determine the most appropriate test for your care (whole genome, RNA sequencing, metabolic studies, other).
3How long does it take to get my results?
The time it takes to get test results back depends on the test. It generally takes between two weeks to one month to receive test results.
4What is the consultation cost?
It is $499 for the initial visit and $299 for the follow-up.
5What is the genetic test cost?
This depends on the specific test. All tests are offered in collaboration with the best US CLIA/CAP certified genetic laboratories. Our clients pay the test in advance and before ordering. Please, see pricing in genetic testing. Payment plans are not available currently.
6How can I pay for your services?
We accept cash, personal check, direct wire transfer, or can bill your credit card with an additional 3.5% convenience fee. The initial visit with Dr. Paul cost is $499 and the follow-up $299. Payment is due at the end of the consultation and is required in full before test ordering, see genetic testing for details.

Services

Genetic Consultation (in-person or online) for
Individuals with a suspected genetic etiology and
  • Adoption or unknown family history
  • Adult complex disorders without diagnosis
  • Adverse medication effects
  • Alport syndrome
  • Alzheimer disease, dementias
  • Autism-spectrum disorders
  • Birth defects and pediatric syndromes
  • Blindness syndromes
  • Cancer predisposition; breast, other
  • Cardiomyopathies, arrhythmias, aneurysms
  • Connective tissue disorders, Marfan syndrome
  • Ehlers-Danlos syndrome
  • Hearing loss
  • Multiple fractures of unknown etiology
  • Other neurological disorders
  • Positive genetic test
  • Precision wellness
  • Positive family history of a rare condition
  • Prion disease (familial type)
  • Renal failure, proteinuria, hematuria
  • Second opinion for genetic cases
  • Seizures and epileptic encephalopathy
  • Skin disorders
  • Genetic testing
  • Whole genome sequencing (WGS)
  • Reanalysis of genome only
  • RNA sequencing for specific cases
  • Expanded newborn screening
  • Metabolic genetic testing
  • Polygenic risk score (PRS)
  • Methylation testing
  • Biological age
  • For more information and pricing go to genetic testing
  • Contact