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19+ Sickle Cell Anemia Hemoglobin Structure Pics

19+ Sickle Cell Anemia Hemoglobin Structure Pics. Sickle cell anemia is an autosomal recessive disorder affecting the function of hemoglobin. However, individuals who are heterozygous (genotype = as).

Haemoglobin S, molecular model Stock Photo: 65208787 - Alamy
Haemoglobin S, molecular model Stock Photo: 65208787 - Alamy from c8.alamy.com
Sickle cell anemia is caused by an abnormal type of hemoglobin called hemoglobin s. At the same time, its epidemiology is a remarkable signature of the past and present world distribution of plasmodium falciparum malaria. Sickling disorder due to hemoglobin s.

Hemoglobin is a protein made of four subunits:

It normally has two alpha chains and two beta chains. The most common form of scd found in north america is homozygous hbs disease (hbss). Sickle cell disease (scd) and its variants are genetic disorders resulting from the presence of a mutated form of hemoglobin, hemoglobin s (hbs) (see the image below). Sickle cell anemia and related abnormalities.

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