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  2. Hemoglobin A - Wikipedia

    en.wikipedia.org/wiki/Hemoglobin_A

    In addition, there is sickle cell trait (HbAS) which is defined by having HbA and HbS. This makes the individual heterozygous for sickle cell. Of the world population, it is estimated that there are about 300 million individuals with the sickle cell trait and about 100 million of those are in sub-Saharan Africa. [18]

  3. Overdominance - Wikipedia

    en.wikipedia.org/wiki/Overdominance

    An example of overdominance in humans is that of the sickle cell anemia.This condition is determined by a single polymorphism.Possessors of the deleterious allele have lower life expectancy, with homozygotes rarely reaching 50 years of age.

  4. Ryan Clark (American football) - Wikipedia

    en.wikipedia.org/wiki/Ryan_Clark_(American_football)

    Clark is involved with sickle cell disease awareness, research, treatment and programming in Pittsburgh. In 2012, he announced the formation of Ryan Clark's Cure League to raise awareness about sickle cell trait and eventually find a cure.

  5. Hemoglobin D-Punjab - Wikipedia

    en.wikipedia.org/wiki/Hemoglobin_D-Punjab

    People with hemoglobin D trait do not have Hemoglobin D disease or sickle cell disease. They cannot develop these diseases later in life. They cannot develop these diseases later in life. While Hemoglobin D can be detected without a DNA test, one is needed to ascertain that a person who carries Hemoglobin D carries hemoglobin D-Punjab.

  6. Isosthenuria - Wikipedia

    en.wikipedia.org/wiki/Isosthenuria

    Isosthenuria may be seen in disease states as chronic kidney disease and acute kidney injury in which the kidneys lack the ability to concentrate or dilute the urine and so the initial filtrate of the blood remains unchanged despite the need to conserve or excrete water based on the body's hydration status.

  7. Hemoglobin-G - Wikipedia

    en.wikipedia.org/wiki/Hemoglobin-G

    The trait is normal-functioning and has no known negative effects. [2] The mutation was first discovered in 1971, during the boom of research in to hemoglobin. [3] The push was backed by the desire to research the causes and possibly fight sickle cell anemia and other types of Anemia. Because the strict laws of clinical testing had not existed ...

  8. Congenital hemolytic anemia - Wikipedia

    en.wikipedia.org/wiki/Congenital_hemolytic_anemia

    The underlying cause of sickle cell anemia is the synthesis of aberrant hemoglobin, which attaches to other aberrant hemoglobin molecules inside the red blood cell to undergo rigid deformation. [18] Sickle cell anemia symptoms usually appear around the age of six months. They can change over time and differ from person to person.

  9. Antagonistic pleiotropy hypothesis - Wikipedia

    en.wikipedia.org/wiki/Antagonistic_pleiotropy...

    Strength of natural selection plot as a function of age. The antagonistic pleiotropy hypothesis (APT) is a theory in evolutionary biology that suggests certain genes may confer beneficial effects early in an organism's life, enhancing reproductive success, while also causing detrimental effects later in life, contributing to the aging process.