COOLEY’S ANEMIA

Cooley’s anemia is a hereditary disorder of the blood affecting the production of hemoglobin. which is the protein responsible of carrying oxygen throughout the body. This condition occurs due to a shortage of red blood cells and reuslts to anemia. People from the Mediterranean, like Italians and Greeks, as well as those from Arabia, Iran, Africa, Southeast Asia, and China, are most likely to have it.

Cooley’s anemia is typically diagnosed in early childhood and necessitates ligelong treatment. Without treatment, Cooley’s anemia can lead to more serious health problems, including organ damage and early death.

SYMPTOMS

Children born with this type will show signs of it early on, such as:

  • Pale skin
  • Fussy
  • Having little hunger
  • Having a lot of illnesses
  • Over time, more signs will show up, such as:
  • Growth slowed
  • Belly (abdominal) swells
  • Yellow skin (jaundice)

Furthermore, if no therapy is received, bones might become fragile, brittle, and malformed.

DIAGNOSIS

People with Cooley’s anemia are more likely to be of Greek, Italian, African, or Asian descent. Most diagnoses are made between the ages of 6 and 12.

These examinations may reveal if you are a carrier and may convey the condition to your offspring:

  • Complete blood count (CBC). This examination measures the size, quantity, and maturity of certain blood cells in a predetermined amount of blood.
  • Hemoglobin electrophoresis. The various forms of hemoglobin are identified by this lab test.

One blood sample may be used for all of these investigations. The infant may be identified during pregnancy by amniocentesis or CVS (chorionic villus sampling).

TREATMENT

Treatment will be determined by your symptoms, age, and overall health. Furthermore, it will depend on how serious the problem is.

Treatment options include:

  • regular transfusions of blood
  • drugs that lower excess iron in your body (also known as iron chelation treatment)
  • Surgical removal of the spleen may be required.
  • Folic acid daily
  • operative gallbladder removal
  • regular evaluations of liver and heart health
  • genetic analyses
  • transplanting bone marrow

Furthermore, avoid using iron supplements. This is because frequent transfusions can cause the accumulation of iron in the heart and other organs, which can lead to organ damage and heart failure.

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