Rare Genetic Diseases
Numerous suspected cases of genetic disorders endure undiagnosed or misdiagnosed due to the absence of connected clinical as well as diagnostic assets in the region, bring about patients to face an immense psycho-socio-economic emergency and numerous a time suffer long-lasting with their ailment. The disorganization that affects one child can be very dissimilar from how it affects another. They are different cause of rare diseases mainly the genetic growth directly caused by chromosomes in some cases it may also cause from one generation to another generation.
- Polymelia
- Neurofibromatosis
- Diprosopus
Related Conference of Rare Genetic Diseases
August 25-26, 2025
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Rare Genetic Diseases Conference Speakers
Recommended Sessions
- Allergic and Immunologic Disorders
- Future Hereditary of Orphan Drugs
- Mystery Diagnosis of Rare Diseases
- Paediatric rare diseases
- Rare Endocrine Genetic Diseases
- Rare Obesity and Metabolic Disorders
- Clinical Research and Public Awareness
- Neglected Rare Tropical Diseases
- Orphan diseases and public health
- Orphan Drugs Treatment for Rare Diseases
- Orphan Drugs- Development Trends and Strategies
- Rare Bacterial, Viral and Fungal infections
- Rare Diseases of Genitourinary System
- Rare Genetic Diseases
- Rare Gynaecological and Obstetrical Diseases
- Rare Oral Diseases and Rare Aging Diseases
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- Translational Medicine - TRANSLATIONALMEDICINE 2025 (UAE)
- Translational of Animal Models to the Clinic - TRANSLATIONALMEDICINE 2025 (UAE)
- Translational Therapeutics and Technologies - TRANSLATIONALMEDICINE 2025 (UAE)
- Treatment & Safe Care - Patient Safety Congress 2025 (Italy)
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- Women's Health & Reproductive Medicine - Medicalresearch-2025 (Netherlands)
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