Clinicians
Cardiovascular genetics
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Family history of a cardiac condition
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Cardiomyopathy and Heart failure
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Thoracic aortic aneurysm or unusual history of aneurysms
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Arrhythmias
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Cardiac arrest
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History of sudden death
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Severe hyperlipidemia or familial hyperlipidemia
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Coronary Artery Disease
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
