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.
Related Conference of Mystery Diagnosis of Rare Diseases
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
- Neglected Tropical Diseases
- Orphan diseases and public health
- Orphan Drug
- Rare Autoimmune Diseases
- Rare Diseases
- Rare Endocrine Genetic Diseases
- Rare Genetic Diseases
- Rare Hematology Diseases
- Rare Neurological Disorders
- Rare Obesity and Metabolic Disorders
- Rare Pediatrics Diseases
- Rare Skin Diseases
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