Sickle-cell anaemia is a genetic blood disorder caused by a mutation in the haemoglobin gene. It causes red blood cells to become misshapen and block small blood vessels, leading to pain and anaemia. If both parents are carriers of the sickle-cell allele, there is a 25% chance their child will have sickle-cell anaemia, as shown through a Punnett square. Treatments aim to prevent pain crises and complications but do not cure the condition, though bone marrow transplants potentially offer a cure.
2. What is It?
A genetic disorder which causes some red
blood cells to go out of shape.
It is caused by a faulty recessive allele
which codes for haemoglobin (protein that
carries o2 found in blood).
3. How is it Passed on?
QUESTION
If both the mother and father is a carrier of
sickle-cell allele, what is the likelihood that
their child would get sickle-cell anaemia?
Fill in the punnet square to show all options.
5. Symptoms?
Severe Pain
sickle cells block tiny vessels
Anaemia
damaged cells cant be replaced fast enough by
the spleen
Tiredness
because of shortage of oxygen
6. Advantages
A carrier of sickle-cell anaemia is less likely to catch
malaria. A carriers condition is known as sickle-cell trait.
The frequency of the sickle-cell allele is higher in places
with a high count of malaria.
This process is called natural selection.
People who have one or two sickle-cell alleles have a
much higher resistance against malaria then those who
have two normal haemoglobin alleles.
7. Treatments?
Most treatments avoid crisis and pain, but do
not cure sickle-cell anaemia. Usually, doctors
prescribe
Antibiotics-to avoid infection
Pain relieving medications
There is a possible cure- bone marrow
transplant, however there is a risk of death in
this procedure.