Q & A: All you need to know about sickle cell anemia

Health and Medical

Anemia is a genetic disorder of hemoglobin in the blood, and requires the inheritance of two sickle cell genes. Here is all you need to know about sickle cell anemia

Sickle cell anemia

Q: What is anemia?

A: Anemia According to the site report " medicinenet"Is a blood disorder caused by abnormal hereditary hemoglobin, and irregular sickle cells can block blood vessels causing damage to tissues, organs and pain.

Anemia is one of the most common hereditary anemia, primarily affecting Africans and African Americans.

Sickle cell anemia

Q: Symptoms and Signs of Angele Anemia?

A: All the main symptoms of hemangiomas are the direct result of abnormal red blood cells that prevent the blood flow that spreads through the body tissues due to hypoxia.

Key features and symptoms of anemia include:

Fatigue and anemia.

the pain.

Swelling, inflammation of the hands or feet and arthritis.

Bacterial infections.

Sudden blood pool in spleen and liver congestion.

Heart and lung injury.

Leg ulcers.

Eye damage.

Mengeal anemia is usually evident in the first year of life. Infants and young children may suffer from fever, abdominal pain, pneumococcal infections, painful swelling of the hands and feet

Sickle cell anemia

Q: How does hemangioma occur?

A: Anemia is inherited, which means that the gene can be transmitted from one parent to the fetus, if the sickle cell must inherit from both mother and father, so that the child has sickle genes.

The inheritance of a single gene is called a sickle trait, so people with sickle cell features usually do not have many symptoms of the disease.

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