For patients living with Ehlers-Danlos syndrome, Marfan syndrome, hereditary cancer risk, and complex genetic conditions — expert virtual consultations with a physician who understands. Introductory consultations: $100.
No referral needed · $100 introductory rate · Response within 48 hours
Dr. Sigireddi's team will reach out within 48 hours to discuss your situation and schedule your consultation. We look forward to speaking with you.
The full spectrum — hEDS, classical, vascular. Including hypermobility spectrum disorder and POTS overlap.
Aortic root surveillance, FBN1 testing, management planning, and coordination with cardiology.
BRCA1/2 interpretation, risk stratification, and guidance on prophylactic options.
MLH1, MSH2, MSH6, PMS2 variant interpretation and colorectal cancer surveillance planning.
Hypertrophic cardiomyopathy, long QT syndrome, familial hypercholesterolemia and related disorders.
For patients who've had normal tests everywhere else. Sometimes the answer requires a geneticist.
Fill out a short form. No medical records needed upfront. Just tell us what you're dealing with.
Dr. Sigireddi personally reviews every request. You'll hear back within 48 hours to schedule your consultation.
A thorough virtual consultation, 60–90 minutes, with a written summary and next-step recommendations provided afterward.
Dr. Meenakshi Sigireddi is one of a small number of physicians in the United States who is double board-certified in both Clinical Genetics & Genomics and Internal Medicine. She currently serves as Director of the High Risk Cancer Genetics Program at NYU Langone's Perlmutter Cancer Center.
Her clinical focus spans hereditary cancer syndromes, connective tissue disorders, and rare undiagnosed conditions. She understands that many patients arrive after years of searching — and that a genetics consultation isn't just about a test result, it's about finally having someone who can see the full picture.
She has personal experience with rare genetic disease in her family, including a family member with osteopetrosis — a condition affecting approximately 1 in 100,000 people — which informs her deep commitment to patients who have been told their symptoms are unexplained.
If you've been searching for answers, dismissed by doctors, or stuck on a 9-month waitlist — this is what we're here for. 60–90 minutes with a board-certified geneticist for $100.
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