Sickle Cell Anaemia
Sickle-cell disorder takes place when someone inherits two bizarre copies of the hemoglobin gene, one from each parent. This gene takes place in chromosome eleven. Several subtypes exist, relying on the exact mutation in every hemoglobin gene. An assault may be activated by using temperature modifications, strain, dehydration, and high altitude. An individual with an unmarried extraordinary reproduction does not commonly have symptoms and is stated to have sickle-cell trait.
- Signs and symptoms
- Genetics OF sickle Cell Anaemia
- Pathophysiology of sickle-cell disease.
- Diagnosis of Sickle Cell Diseases
Related Conference of Sickle Cell Anaemia
March 09-10, 2026
21th World Congress on Tissue Engineering Regenerative Medicine and Stem Cell Research
Singapore City, Singapore
June 18-19, 2026
16th International Conference on Human Genetics and Genetic Diseases
Singapore City, Singapore
June 18-19, 2026
19th International Conference on Genomics & Pharmacogenomics
Singapore City, Singapore
Sickle Cell Anaemia Conference Speakers
Recommended Sessions
- Cancer Genomics
- Cytogenetics and Neurogenetics
- Gene Therapy and Genetic Counselling
- Nutrigenetics
- Epigenetics
- Genetic Disorders
- Genome Engineering
- Genome Mapping
- Genomics Market
- Human Genetics and Genomics
- Immunology and Immunogenetics
- Medicinal Genetics
- Molecular and Cellular Genetics
- Pharmacogenomics
- Sickle Cell Anaemia
- Stem Cell Biology
- Stem Cell Therapy
- Thalassemia
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