Clinicians
Cancer genetics
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Family history of a known mutation in a cancer predisposition gene
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Individuals of Ashkenazi Jewish ethnicity known to be at increased risk for cancer predisposition
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Cancer at a young age less than 50 years
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Multiple primary cancers in a single individual
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Bilateral or multifocal cancers
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Same type of cancer in close relatives (same side of a family)
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Rare tumors (e.g. retinoblastoma, adrenocortical carcinoma)
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Unusual cancer presentation
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Uncommon tumor histology
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Rare cancers known to be associated with genetic syndromes
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Breast, ovarian, fallopian tube, or primary peritoneal cancer
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Uterine cancer
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Thyroid cancer
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Pancreatic cancer
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Prostate cancer
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Bone cancer
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
