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- Q1642147 subject Q7215597.
- Q1642147 subject Q8382032.
- Q1642147 abstract "Haemoglobinopathy is a kind of genetic defect that results in abnormal structure of one of the globin chains of the hemoglobin molecule. Hemoglobinopathies are inherited single-gene disorders; in most cases, they are inherited as autosomal co-dominant traits. Common hemoglobinopathies include sickle-cell disease. It is estimated that 7% of world's population (420 million) are carriers, with 60% of total and 70% pathological being in Africa. Hemoglobinopathies are most common in ethnic populations from Africa, the Mediterranean basin and Southeast Asia.Hemoglobinopathies imply structural abnormalities in the globin proteins themselves. Thalassemias, in contrast, usually result in underproduction of normal globin proteins, often through mutations in regulatory genes. The two conditions may overlap, however, since some conditions which cause abnormalities in globin proteins (hemoglobinopathy) also affect their production (thalassemia). Thus, some hemoglobinopathies are also thalassemias, but most are not.Either hemoglobinopathy or thalassemia, or both, may cause anemia. Some well-known hemoglobin variants such as sickle-cell anemia and congenital dyserythropoietic anemia are responsible for diseases, and are considered hemoglobinopathies. However, many hemoglobin variants do not cause pathology or anemia, and thus are often not classed as hemoglobinopathies, because they are not considered pathologies. Hemoglobin variants are a part of the normal embryonic and fetal development, but may also be pathologic mutant forms of hemoglobin in a population, caused by variations in genetics. Other variants cause no detectable pathology, and are thus considered non-pathological variants.".
- Q1642147 wikiPageWikiLink Q12156.
- Q1642147 wikiPageWikiLink Q1571741.
- Q1642147 wikiPageWikiLink Q17022356.
- Q1642147 wikiPageWikiLink Q17022368.
- Q1642147 wikiPageWikiLink Q185034.
- Q1642147 wikiPageWikiLink Q185137.
- Q1642147 wikiPageWikiLink Q192120.
- Q1642147 wikiPageWikiLink Q207843.
- Q1642147 wikiPageWikiLink Q2297155.
- Q1642147 wikiPageWikiLink Q2873354.
- Q1642147 wikiPageWikiLink Q33829.
- Q1642147 wikiPageWikiLink Q3518755.
- Q1642147 wikiPageWikiLink Q409030.
- Q1642147 wikiPageWikiLink Q409202.
- Q1642147 wikiPageWikiLink Q412234.
- Q1642147 wikiPageWikiLink Q43041.
- Q1642147 wikiPageWikiLink Q5160422.
- Q1642147 wikiPageWikiLink Q5712484.
- Q1642147 wikiPageWikiLink Q5712491.
- Q1642147 wikiPageWikiLink Q6531938.
- Q1642147 wikiPageWikiLink Q7187.
- Q1642147 wikiPageWikiLink Q7208.
- Q1642147 wikiPageWikiLink Q7215597.
- Q1642147 wikiPageWikiLink Q748442.
- Q1642147 wikiPageWikiLink Q8054.
- Q1642147 wikiPageWikiLink Q8382032.
- Q1642147 wikiPageWikiLink Q848343.
- Q1642147 wikiPageWikiLink Q964797.
- Q1642147 comment "Haemoglobinopathy is a kind of genetic defect that results in abnormal structure of one of the globin chains of the hemoglobin molecule. Hemoglobinopathies are inherited single-gene disorders; in most cases, they are inherited as autosomal co-dominant traits. Common hemoglobinopathies include sickle-cell disease. It is estimated that 7% of world's population (420 million) are carriers, with 60% of total and 70% pathological being in Africa.".
- Q1642147 label "Hemoglobinopathy".