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Sickle-cell anemia is characterised by abnormal haemoglobin which are not the correct shape and cannot carry oxygen.
It is a genetic disease - and a person must have two copies of the gene to have sickle-cell anemia. (Heterozygous individuals, with one copy, are known as having sickle-cell trait - and some of their haemoglobin may be misshapen).
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BeauSickle cell disease is a genetic disorder where red blood cells take on a "sickle" shape, causing blockages in blood vessels and leading to various complications. It is inherited in an autosomal recessive manner, meaning a child must inherit a sickle cell gene from both parents to develop the disease.
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An inherited disease or disorder that is caused by a mutation in a gene or by a chromosomal defect?
There are many thousands of different mutations.
Is Canavan disease inherited?
Yes, Canavan disease is an inherited genetic disorder caused by mutations in the ASPA gene. It is inherited in an autosomal recessive pattern, meaning that an individual must inherit two copies of the mutated gene (one from each parent) to develop the disease.
Is sickle cell anemia a communicable or noncommunicable?
I don't know what a communitive disease is, and neither does the dictionary, but sickle cell anemia is an inherited abnormality. I hope that helps.If you are asking if sickle cell is a disease in which you can catch from other people. The answer is No. It is an inherited Blood disorder.
What movement disorders are caused by inherited genetic defects.?
Movement disorders caused by inherited genetic defects include Huntington's disease, spinocerebellar ataxias, dystonias, and certain forms of Parkinson's disease. These disorders result from specific genetic mutations that can be passed down from parents to their children. Symptoms may vary depending on the specific disorder but often involve involuntary movements, tremors, or muscle stiffness.
A person who has inherited the autosomal recessive disorder called?
A person who has inherited an autosomal recessive disorder will have two copies of the mutated gene, one from each parent. This results in the individual expressing the disorder. Symptoms can vary depending on the specific disorder.
