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

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