thalassaemia

Inherited anemia condition

Thalassaemia is a hereditary blood disorder in which the body produces abnormal hemoglobin, leading to anemia.

The condition ranges from mild to severe; major forms require regular blood transfusions.

It occurs most commonly in people of Mediterranean, Middle Eastern, African, and Southeast Asian descent.

Also spelled thalassemia.

genetics

mutation

Permanent DNA alteration

genetic counseling · prenatal diagnosis · consanguinity · pedigree · genotype · silent carrier · deletion · point mutation

treatment

transfusion

Transfer of blood intravenously

gene therapy · folic acid · ferritin · blood bank · matched donor · supportive care

Mediterranean

Greece

Balkan peninsula nation

  • ItalyBoot-shaped European nation
  • CyprusMediterranean island nation
  • SardiniaItalian autonomous island region

Sicily · Crete · Malta · Middle East · Southeast Asia · South Asia · selective pressure · migration patterns · consanguinity

hematology

hemoglobin

Erythrocyte's oxygen-binding protein

hematopoiesis · blood smear

symptoms

fatigue

Weariness from prolonged exertion

dizziness · heart palpitations · jaundice · bone deformities · hepatomegaly · osteoporosis · leg ulcers · gallstones · delayed puberty

Family

thalassic, thalassemia

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Timeless · Negative · Rated G