Mystery Diagnosis of Rare Diseases
Rare diseases affect an estimated 2-4% of the population. A likely next step is whole genome sequencing, a diagnostic technique that over the last decade has significantly bolstered the effort to identify undiscovered diseases. A different approach is to search for patients with similar hereditary abnormalities and similar side effects. Determining the cause of a malady is often a victory in its own right for people who’ve spent years trying to figure out what’s wrong with their bodies.
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Mystery Diagnosis of Rare Diseases Conference Speakers
Recommended Sessions
- Allergic and Immunologic Disorders
- Challenges of Living with Rare Diseases
- Clinical Research and Treatment
- Future of Rare Diseases Research
- Gene Therapy for Rare Diseases
- Infectious Diseases
- Mystery Diagnosis of Rare Diseases
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- Rare Autoimmune Diseases
- Rare Diseases
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- Rare Hematology Diseases
- Rare Neurological Disorders
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- Rare Skin Diseases
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