thalassemia

Inherited anemia condition

Thalassemia is an inherited blood disorder in which the body produces abnormal hemoglobin, leading to anemia and other complications.

The severity ranges from mild forms requiring no treatment to major forms necessitating regular blood transfusions.

Named from the Greek word for sea, it was first identified in populations around the Mediterranean but occurs worldwide.

Couples with thalassemia trait may undergo genetic counseling before having children.

symptoms

pallor

Unhealthy facial whiteness

dizziness · jaundice · hepatomegaly · bone deformities · failure to thrive · irritability · poor appetite · leg ulcers · dark urine

genetic

inheritance

Property received from ancestors

genetic counseling · prenatal testing · screening · pedigree · family history · chromosomes · alleles · genotype · phenotype · hereditary

blood

hemoglobin

Erythrocyte's oxygen-binding protein

complete blood count

geography

Mediterranean

Sea between Europe, Africa, Asia

  • GreeceBalkan peninsula nation
  • ItalyBoot-shaped European nation
  • CyprusMediterranean island nation

Sardinia · Sicily · Southeast Asia · Thailand · India · Middle East · Africa · China · endemic · malaria

treatment

transfusion

Transfer of blood intravenously

bone marrow transplant · stem cell transplant · folic acid · gene therapy · monitoring

complications

cardiomyopathy

Heart muscle disorder

hypogonadism · osteoporosis · cirrhosis · gallstones · thrombosis · infections · delayed puberty

Opposites
health status

thalassemiahealth

Condition of body, mind

hemoglobin production

thalassemiapolycythemia

Elevated red cell count

type of hemoglobin disorder

thalassemiasickle cell disease

Hereditary anemia with misshapen erythrocytes

sickle cell anemia

Family

thalassic, thalassaemia

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Top 1,000,000
Profile
Used worldwide · Timeless · Negative · Rated G