Saturday , January 23 2021

The inherited types of blood disease and everything you want to know about them



Hereditary blood disorders are diseases that are genetically transmitted to the family from parents to children, which can affect red blood cells due to genetic defects.

Hereditary blood disorders
Hereditary blood disorders

What are the blood disorders?

Web page "Medical News Today"Blood disorders affect the main components of the blood and include:

– Red blood cells that carry oxygen to the body tissue.

– White blood cells that fight inflammation.

– Thrombocytes, which helps to clot the blood.

– Blood disorders can also affect the flow of blood, called plasma.

Types of Hereditary Blood Diseases

First Thalassemia

Web page "Health line"Talasemia is a hereditary blood disorder in which the body is an abnormal form of hemoglobin, and hemoglobin is a protein found in red blood cells that carry oxygen.

This disorder leads to excessive destruction of red blood cells, leading to anemia, a condition in which your body does not produce enough red blood cells.

Thalassemia is inherited, meaning that at least one of your parents must be the carrier of the disease, either because of genetic mutation or deletion of certain parts of the major genes.

Thalassemia of genetic diseases
Thalassemia of genetic diseases

Symptoms of thalassemia

Symptoms of thalassemia may vary, and the most common symptoms are:

– Abnormal bone, especially in the face.

– dark urine.

– Late growth.

Fatigue and exaggerated fatigue.

– Yellow or pale skin.

Treatment of thalassemia

Since thalassemia is a genetic disorder, there are no ways to prevent it. However, there are ways you can control the disease to prevent complications.

Low fat, vegetarian diet is the best choice for most people, including those suffering from thalassemia. Limit foods rich in iron if you already have a high level of iron in the blood. The exercise is light.

Hemophilia of hereditary blood diseases
Hemophilia or blood flow from genetic diseases of the blood

II Hemophilia

Hemophilia is a hereditary blood disease in which a person has low levels of certain proteins called "clotting factors", leading to excessive bleeding, blood clotting or blood clotting.

According to the World Federation hemophiliaWFH) One in ten thousand people die of illness.

Hemophilia can not be treated but can be treated to reduce symptoms and prevent future health complications.

Symptoms of haemophilia

The extent of your symptoms depends on the severity of your deficiency, bleeding can occur as follows:

Blood in the urine.

Blood in the chair.

– Big bruises for no reason.

Bleeding gums.

Frequent nose bleeding.

Pain in joints.

Anemia of sickle cell
Anemia of sickle cell

III Serum Cell anemia or sickle cell anemia

According to "Mayo clinic"Anemia is the hereditary form of anemia or anemia, a condition where there is not enough healthy red blood cells to carry enough oxygen throughout the body.

Red blood cells are usually flexible and circular, and easily move through the blood vessels.

In hemangiomas, red blood cells become rigid and sticky and form like serpents. These irregular cells can stumble into small blood vessels that can slow or block the flow of blood and oxygen to the body parts.

There is no cure for most people with anemia, but treatments can alleviate pain and prevent problems related to the disease.

Symptoms of sickle cell anemia

Signs and symptoms of sickle cell anemia, which differ from person to person, include the following:

– Anemia.

– Lack of red blood cells, which causes your body not getting the oxygen it needs to feel energy, causing fatigue and fatigue.

– I feel pain.

Painful swelling in your hands and feet.

– frequent infections.

– Late growth.

Visual problems.

– Unwanted fitting of severe pain, such as abdominal pain, chest, bones or joints.

– Abdominal pain.

– fever.

Face and face watering.



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