Hemoglobinopathies example sentences

Related (1): thalassemia

"Hemoglobinopathies" Example Sentences

1. Hemoglobinopathies are inherited blood disorders.
2. The prevalence of hemoglobinopathies is high in certain ethnic populations.
3. Sickle cell anemia is a well-known hemoglobinopathy.
4. Patients with hemoglobinopathies often require frequent blood transfusions.
5. Hemoglobinopathies can lead to chronic anemia.
6. Thalassemia is another common hemoglobinopathy.
7. Hemoglobin E is a hemoglobinopathy found in Southeast Asia.
8. Diagnosis of hemoglobinopathies involves genetic testing.
9. Hemoglobinopathies can cause a wide range of symptoms.
10. Hemoglobinopathies can be difficult to manage and treat.
11. There are many different types of hemoglobinopathies.
12. Hemoglobinopathies affect the structure of the hemoglobin molecule.
13. Hemoglobinopathies are caused by mutations in the hemoglobin genes.
14. Hemoglobinopathies can be inherited in an autosomal recessive manner.
15. Hemoglobinopathies can cause both acute and chronic complications.
16. There is no cure for hemoglobinopathies.
17. Hemoglobinopathies can affect both adults and children.
18. Hemoglobinopathies are a major public health concern in many countries.
19. Hemoglobinopathies can affect multiple organ systems.
20. Hemoglobinopathies can be associated with increased risk of infections.
21. Hemoglobinopathies can lead to gallstones.
22. Hemoglobinopathies can be managed with regular blood transfusions.
23. Hemoglobinopathies can cause significant morbidity and mortality.
24. Hemoglobinopathies can be complex to diagnose and treat.
25. Hemoglobinopathies can lead to chronic pain and fatigue.
26. Hemoglobinopathies can affect quality of life.
27. Hemoglobinopathies can require long-term medical management.
28. Hemoglobinopathies can be associated with increased risk of stroke.
29. Hemoglobinopathies can be challenging for patients and their families to manage.
30. Hemoglobinopathies can be treated with bone marrow transplantation.

Common Phases

1. Sickle cell disease;
2. Thalassemia;
3. Hemoglobin E disorders;
4. Hemoglobin C disorders;
5. Hemoglobinopathy;
6. Hemoglobin electrophoresis testing;
7. Hemoglobin variants;
8. Beta-thalassemia;
9. Alpha-thalassemia;
10. Hereditary persistence of fetal hemoglobin (HPFH).

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