Ad
related to: thalassemia prevalence by country map location- For Patients
Visit this website if you are a
patient seeking information.
- Sign Up
Stay up to date. Sign up to receive
the latest thalassemia information.
- Emerging NTD Data
See how hemoglobin levels
affect NTD patients.
- Management
Find the latest thalassemia
management guidelines.
- For Patients
Search results
Results from the WOW.Com Content Network
β thalassemia major (Mediterranean anemia or Cooley anemia) is caused by a β o /β o genotype. No functional β chains are produced, and thus no hemoglobin A can be assembled. This is the most severe form of β-thalassemia. β thalassemia intermedia is caused by a β + /β o or β + /β + genotype. In this form, some hemoglobin A is produced.
Alpha thalassemia is has greatest prevalence in populations originating from Southeast Asia, Mediterranean countries, Africa, the Middle East, India, and Central Asia. [7] Having a mild form of alpha thalassemia has been demonstrated to protect against malaria and thus can be an advantage in malaria endemic areas. [12]
Beta-thalassemia; Other names: Microcytemia, beta type [1] Beta thalassemia genetics, the picture shows one example of how beta thalassemia is inherited. The beta globin gene is located on chromosome 11. A child inherits two beta globin genes (one from each parent). Specialty: Hematology: Types: Thalassemia minor, intermediate and major [2] Causes
This list concerns blood type distribution between countries and regions.Blood type (also called a blood group) is a classification of blood, based on the presence and absence of antibodies and inherited antigenic substances on the surface of red blood cells (RBCs).
Therefore, most transfusion-dependent thalassemia patients can be diagnosed within the first few years of life, which severe anemia, differed growth, jaundice and hepatosplenomegaly can be observed. Parameters for confirmation includes baseline hemoglobin level <7g/dL, enlargement of liver and spleen (>5 cm) and height in the first 10th percentile.
Country / territory Rate [1] Lithuania 15.16 Serbia 15.12 Romania 14.92 Latvia 14.69 Bulgaria 14.31 Ukraine 13.70 Russia 13.27 Estonia 13.13 Croatia 12.98 Hungary
The Mentzer index, described in 1973 by William C. Mentzer, [1] is the MCV divided by the RBC count. It is said to be helpful in differentiating iron deficiency anemia from beta thalassemia trait.
This is a list of countries by risk of premature death from non-communicable disease such as cardiovascular disease, cancer, diabetes, or chronic respiratory disease between ages 30 and 70 as published by the World Health Organization in 2008. Measuring the risk of dying from target NCDs is important to assess the extent of burden from ...
Ad
related to: thalassemia prevalence by country map location