Sickle cell anemia is also known as sickle cell disease or sickle cell disorder.
A child with SC genotype inherits one sickle cell gene and one gene for hemoglobin C, while a child with SS genotype inherits two sickle cell genes. SC genotype typically results in milder symptoms compared to SS genotype, which is associated with more severe complications such as frequent pain crises and organ damage. Both genotypes can still lead to sickle cell disease and require management and monitoring.
"AS" and "SS" refer to specific genotypes of the hemoglobin gene. "AS" indicates a carrier of sickle cell trait, while "SS" indicates someone with sickle cell disease. Both conditions involve abnormal hemoglobin and can have significant health implications.
SS,Ss
The parents are both recessive (Ss) for sickle cell anemia.
The parents are both recessive (Ss) for sickle cell anemia.
Sickle cell is not a germ, it's a disease! The spreading of this disease occurs when two people carry the trait of sickle cell in their genetic makeup and they have children. The odds of any child born to parents who carry the trait are different each time. 50% can be born with just trait, 1 out of 4 will be born with Sickle Cell Anemia and 1 out of 4 will be born without anything. Then there are varied levels of Sickle Cell, there's Anemia (SS), Disease (SC). it is heredity
The parents are both recessive (Ss) for sickle cell anemia.
Yes, the genotype SC refers to individuals who have inherited one sickle cell allele (S) and one C allele, resulting in a sickle cell trait that is different from having sickle cell disease. This genotype can lead to some symptoms similar to sickle cell disease under certain conditions.
It is also called sickle cell anemia, sicklemia, or SS disease
It is also called sickle cell anemia, meniscocytosis, or sicklemia
It is also called sickle cell anemia, meniscocytosis, or SS disease