sickle-cell anemia in English
Use "sickle-cell anemia" in a sentence
1. Sickle-cell anemia.
2. Children inherit sickle-cell anemia from both parents.
3. Sickle-Cell Anemia—Knowledge Is the Best Defense
4. I lost my younger brother to sickle-cell anemia.
5. Although she suffers from sickle-cell anemia, she counts her blessings.
6. Those with sickle-cell anemia should also have regular medical checkups.
7. Carmen, mentioned above, read books on sickle-cell anemia, as did her parents.
8. Perhaps you have heard of what we call beta thalassemia, or sickle- cell anemia.
9. A highly sensitive and very rapid prenatal test for sickle-cell anemia has been introduced.
10. 18 Sickle - cell anemia affects a red blood cell's oxygen carrying capacity, making everyday tasks difficult.
11. The sickle cell anemia (HbS/S) was diagnosed only after the abruptio placentae had been performed.
12. By carefully following such guidelines, it is possible for many with sickle-cell anemia to live normal, happy lives.
13. I know it's possible, but it's rare, like tay-Sachs disease in the Jewish population or sickle cell anemia in African-Americans.
14. People who have AA blood can be assured that none of their children will develop sickle-cell anemia, no matter whom they marry.
15. Antimetabolites Antimetabolites are used to treat leukemia, skin cancer, ovarian cancer, leukemia, thrombocythemia, skin cancer, melanoma, rheumatoid arthritis, organ transplant, and sickle cell anemia
16. When proteins have defects in the amino acid chain or are incorrectly folded, they can cause a number of diseases, including sickle-cell anemia and cystic fibrosis.
17. As seen in cases of Mendelian diseases, such as sickle cell anemia or thalassemias, heterozygous carriers may have selective advantages, in this particular case a natural resistance against Malaria tropica.
18. Today, Crispr Cas9, the most popular form of the powerful gene-editing technology, is widely used to accelerate experiments, grow pesticide-resistant crops, and design drugs to treat life-threatening genetic diseases like sickle cell anemia
19. Due to migration of inhabitants from high-risk areas for hemoglobin diseases, primarily Africa, South East Asia and Mediterranean countries, the importance of sickle cell anemia, hemoglobin (Hb) E thalassemia and other hemoglobin diseases in Germany is also increasing.
20. Persons at increased risk for infection or more severe disease include infants; the elderly; persons with achlorhydria; those receiving immunosuppressive therapy; persons who may have received antimicrobials for another illness; and those persons with sickle-cell anemia, cancer, or acquired immunodeficiency syndrome.