Precision Care
Precision care considers all aspects of your life to develop the most effective care plan. It considers factors such as age, environment, family history, and lifestyle to tailor a treatment specifically to you.
A key component of precision care is understanding your genome, which reveals what makes you unique.
Genomic sequencing plays a crucial role in this process by analyzing your genetic makeup to optimize your care. This involves identifying genetic mutations that cause medical conditions and recognizing genetic risk factors, which inform lifestyle and environmental recommendations to enhance health.
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
