sickle cell is an inherited blood disease that affect hemoglobin the molecule in red blood cell that deliver oxygen to cell through out the body.people with this disorder have typical hemoglobin molecule that called hemoglobin S, which can turn red blood cell to sickle cell anemia shape.

what is sickle cell disease ?

sickle cell disease is caused by defected called mentions in the beta goblin gene that make hemoglobin normally in the red blood cells take up to all oxygen in the lung and carries it through the arteries genetic.

what cause sickle cell disorder?

Practically all of the major symptoms of sickle cell anemia are the direct result of the abnormally sickle cell, red blood cells blocking the flow of blood that circulates through the tissues.furthermore the pain of the sickle cell disease is very excruciating .

Symptoms of sickle cell disorder

Main symptoms of sickle cell disorder

Main symptoms of sickle cell are very personal to personal and change over time, including Episodes pf pains ,painful swelling of hands and feet ;frequent of infection,delayed problem plus vision issue.

How to diagnose with sickle cell disease?

when portal blood flow to liver is alerted (like portal hypertension).Anemia blood rise.

what body system does sickle cell affect?

Any body system can be affect by sickle cell, however there are the major of body system that are always affect by sickle cell such as cardiovascular,muscular,skeletal,sensory,nervous,and urinary system.

Main organ that are affect by sickle cell illness.

The main organs are affected by sickle cell disease.

the liver ,heart,kidneys.gallbladder ,eyes, bones, and joints can suffer damage from the abnormal function of the sickle cells and their inability to flow the small blood vessels correctly.

The body part(organs) that affected by sickle cell disease.

If a person have sickle cells disease their life will be brimming with pain all the time. Because sickle cells are not flexible and can stick to vessel walls, causing blockage that slow or stop the flow of blood .when this happens, oxygen is unable to reach nearby tissues.The lack of oxygen in tissue can cause attacks of sudden server pain called pain crises.

What would happen to someone who are dealing with sickle cell?

A sickle cell crisis is pain that can begin suddenly and last several hours to days. It happen when sickle red blood cell block small blood vessels that carry blood to your bones. you might have in your back, knees ,legs,arms,chest,or stomach.The pain can be throbbing ,sharp,dull or stabbing.

What is pain crisis ?

The only treatment that offers a potential cue for sickle cell anemia is seem to be stem or cells translation. The aims to replace the source of new red blood cells, stem cell in the bone marrow , with healthy stem cells from a matching donor,this treatment is not available to everyone because it can be very difficult to find a suitable donor.IN addition, there are several approved medication to improve the symptoms of sickle cell anemia. These are hydroxyurea and endari(L- glutamine).

What is the treatment of sickle disease ?

if a sickle cell disease left untreated you will have a difficulty of breathing and fatigue are common symptoms of this condition ,which can be fatal organ damage.Sickle cells that block blood flow vessels immediately deprive the affected organ of blood and oxygen Ulatmily you may dies.

What could happen if sickle cell disorder left untreated?

How does sickle cells affect blood flow?

Sickle cells will block blood flow through blood vessels immediately deprive the affect ed organ of blood and oxygen.Chronic deprivation of oxygen _rich blood can damage nerves and organs in your body ,including kidneys ,liver and spleen.

How the sickle cells affected the blood flow.

Sickle cells anemia can be prevented while persona; risk factors for developing sickle cells are out of control,it is possible to avoid passing the disease down genetically. For instance ,genetic counselor can advise you if plan to have child and carry the sickle cell trit.

Some preventable measures of sickle cell disorder