sickle cell anaemia

Inherited blood disease

Sickle cell anaemia is a hereditary blood disorder in which red blood cells become rigid and crescent-shaped, obstructing blood flow and causing pain, organ damage, and shortened lifespan.

The condition predominantly affects people of African, Mediterranean, and South Asian descent.

Carriers of a single gene copy have some resistance to malaria, explaining the trait's persistence in populations from malaria-endemic regions.

blood

hemoglobin

Erythrocyte's oxygen-binding protein

hematocrit · bilirubin · jaundice · hypoxia · ischemia · bone marrow · transfusion · blood count

genetics

inheritance

Property received from ancestors

genotype · phenotype · mutation · point mutation · nucleotide · substitution · codon · chromosome · DNA · genetic counseling

treatment

blood transfusion

Infusing donated cells intravenously

pain management · gene therapy · immunization · hydration · oxygen therapy

complications

stroke

Sudden brain blood blockage

retinopathy · kidney damage · osteomyelitis · infection · sepsis · organ damage · pneumonia

chronic

lifelong

Lasting entire existence

monitoring · hospitalization · outpatient · healthcare · quality of life · caregiver · support · adaptation · resilience · disability

pain

crisis

Decisive dangerous moment

bone pain · joint pain · abdominal pain · chest pain · opioids · analgesics · acute · chronic pain · inflammation · suffering

Opposites
genetic vs acquired disease origin

sickle cell anaemiainfectious disease

Pathogen-caused transmissible ailment

occupational disease · food poisoning · lifestyle disease · malaria · HIV/AIDS

disease curability

sickle cell anaemiabacterial infection

Illness from harmful microorganisms

strep throat · acute illness · appendicitis · broken bone · pneumonia

blood cell morphology

sickle cell anaemiagood health

Absence of illness

Family

sickle, anaemia, anemia, sickled, sickles, sickling, celled, cellular, cellar

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