Disclaimer
We’re actively expanding Guideline Genius to cover the full UKMLA content map. You may notice some conditions not uploaded yet, or articles that only include diagnosis and management for now. For updates, follow us on Instagram @guidelinegenius.
We openly welcome any feedback or suggestions through the anonymous feedback box at the bottom of every article and we’ll do our best to respond promptly.

Thank you for your support.
The Guideline Genius Team

Total Live Articles: 323

Thalassaemia

Thalassaemia is a group of hereditary haemoglobin disorders, caused by autosomal recessive mutations in the alpha or beta globin chains:

  • Mutation in alpha globin chain → alpha thalassaemia
  • Mutation in beta globin chain → beta thalassaemia

Quick comparison:

  • Alpha thalassaemia is more common, and typically has a lower disease burden
  • Beta thalassaemia is less common, and typically has a higher disease burden (severe and transfusion-dependent disease)

Alpha Thalassaemia

Aetiology

Autosomal recessive condition [Ref]

  • Most common: deletion of one or more of the 4 alpha globin genes, on chromosome 16
  • Less common: non-deletional mutation (less common but associated with more severe disease)

In contrast, point mutation is more common in beta thalassaemia (than deletional mutation).

Epidemiology

Alpha thalassaemia is more prevalent than beta thalassaemia (5% vs 1.5%) [Ref]

Thalassaemia is more prevalent in: [Ref]

  • Mediterranean
  • Southeast Asia
  • Middle East
  • Indian subcontinent and sub-Saharan Africa

There is a documented evolutionary association between the thalassaemia carrier state and resistance to malaria, which explains why the disease is highly prevalent in regions where malaria was or remains common. [Ref]

Classic textbook epidemiological associations:

  • Thalassaemia → Mediterranean / Middle Eastern / Asian
  • Sickle cell → African / Afro-Caribbean

Types and Clinical Manifestation

Based on the number of defective alpha globin alleles, there are 4 forms of alpha thalassaemia: [Ref1][Ref2][Ref3]

Form Genetic Clinical manifestation
Minima (silent carrier) 1 defect (-α/αα)
  • Usually asymptomatic
  • No anaemia
Minor (trait) 2 defects (-α/-α or –/αα)
  • Usually asymptomatic
  • Mild anaemia possible
Intermediate (Hb H disease) 3 defects (–/-α) Variable clinical presentation (more severe in non-deletional variants):

  • Jaundice (typically mild)
  • Anaemia
  • Splenomegaly
  • Skeletal changes (e.g. skull bossing, maxilla hypertrophy, prominent malar eminence) (milder than in beta thalassaemia)
Major (Bart’s hydrops fetalis) 4 defects (–/–) Incompatible with life

  • Hydrops fetalis (severe anaemia → heart failure → generalised oedema + pleural and pericardial effusions)
  • Hepatosplenomegaly
  • Death in utero or shortly after birth (due to severe hypoxia)
  • If survived → transfusion-dependent thalassaemia

Maternal complications:

  • Pre-eclampsia
  • Premature delivery
  • Severe anaemia of pregnancy

Investigation and Diagnosis

Laboratory Tests

Thalassaemia causes a microcytic, hypochromic anaemia [Ref1][Ref2]

  • ↓↓ Mean corpuscular volume (microcytic)
  • ↓ Mean corpuscular haemoglobin (hypochromic)
  • Anaemia is typically mild to moderate (only seen in trait and HbH disease)

Mean corpuscular volume and mean corpuscular haemoglobin are often significantly reduced in alpha-thalassaemia.

This reduction is typically disproportionate to the level of anaemia (i.e. the haemoglobin level is typically normal or mildly reduced). [Ref1][Ref2]

Electrophoresis findings: [Ref1][Ref2]

  • Normal HbA2
  • Normal HbF
  • HbH – only present in HbH disease

Normal HbA2 Levels is a critical finding for alpha-thalassaemia, as it helps distinguish it from beta-thalassaemia, where HbA2 is typically elevated.

Confirmatory Test

Gold standard: genetic testing [Ref1][Ref2]

  • Typically PCR to detect the mutation
  • Venous blood can be used for testing

Note that haemoglobin electrophoresis is only used to diagnose beta thalassaemia, it cannot reliably diagnose alpha thalassemia.

Gold standard diagnosis of thalassaemia:

  • Alpha → genetic testing
  • Beta → haemoglobin electrophoresis

Bone marrow analysis is not routinely indicated in thalassaemia and is used only to exclude other haematological diseases.

Management

Form Specific Management

[Ref1][Ref]

Alpha thalassaemia form Management approach
Minima (silent carrier) No treatment is typically required
Minor (trait)
Intermediate (Hb H disease) Largely depends on disease severity:

  • Folic acid supplementation (to support red cell production) – all patients
  • Occasional red cell transfusions (regular transfusions is typically not necessary)
Major (Bart’s hydrops fetalis)
  • Antenatal management → intrauterine transfusion (starting in 2nd trimester)
  • Post-natal management → lifelong regular red cell transfusions and iron chelation therapy OR curative treatment

Genetic counselling, including testing of partners is recommended for all patients due to the autosomal recessive inheritance pattern.

It plays a key role in identifying at-risk couples, assessing the risk of severe disease in offspring (including HbH disease and hydrops fetalis), and facilitating informed reproductive decision-making.

Conditional Management

[Ref]

Management Description / notes
Splenectomy Primary indication: symptomatic splenomegaly
Curative treatment
  • Allogenic haematopoietic stem cell transplantation
  • Gene therapy

Beta Thalassaemia

Aetiology

Autosomal recessive condition [Ref]

  • Most common: point mutation of one or more of the 2 beta globin genes, on chromosome 11
  • Less common: insertion, deletional mutations

In contrast, deletional mutation is more common in alpha thalassaemia (than point mutation).

Thalassaemia is more prevalent in: [Ref]

  • Mediterranean
  • Southeast Asia
  • Middle East
  • Indian subcontinent and sub-Saharan Africa

There is a documented evolutionary association between the thalassaemia carrier state and resistance to malaria, which explains why the disease is highly prevalent in regions where malaria was or remains common. [Ref]

Classic textbook epidemiological associations:

  • Thalassaemia → Mediterranean / Middle Eastern / Asian
  • Sickle cell → African / Afro-Caribbean

Clinical Manifestation

[Ref1][Ref]

Form Genetics Clinical manifestation
Minor (trait) 1 defective allele (heterozygous) Typically asymptomatic
Major 2 defective alleles (homozygous) Considered as transfusion-dependent thalassaemia

  • Early presentation (<2 y/o)
  • Symptomatic, severe anaemia (possibly life-threatening without regular transfusion)
  • Hepatosplenomegaly (due to compensatory extramedullary haematopoiesis)
  • Bone marrow expansion → craniofacial protrusions (e.g. skull bossing, maxilla hypertrophy, prominent malar eminences), bone pain
  • Growth retardation and delayed puberty

Another major complication is chronic iron overload (see separate section below)

Investigation and Diagnosis

Laboratory Tests

Thalassaemia causes a microcytic, hypochromic anaemia [Ref1][Ref2]

  • ↓↓ Mean corpuscular volume (microcytic)
  • ↓ Mean corpuscular haemoglobin (hypochromic)
  • Anaemia
    • Typically mild / none in minor forms
    • Severe anaemia seen in major forms

Mean corpuscular volume and mean corpuscular haemoglobin are often significantly reduced in alpha-thalassaemia.

This reduction is typically disproportionate to the level of anaemia (i.e. the haemoglobin level is typically normal or mildly reduced). [Ref1][Ref2]

Confirmatory Test

Primary confirmatory test: haemoglobin analysis (by haemoglobin electrophoresis or liquid chromatography) [Ref1][Ref2]

  • ↑ HbA2 (>3.5%)
  • ↑ HbF
  • No HbH

Genetic testing is typically used in those who are <12 m/o where haemoglobin analysis may be inconclusive due to physiological haemoglobin switching. [Ref]

Bone marrow analysis is not routinely indicated in thalassaemia and is used only to exclude other haematological diseases.

Management

Form Specific Management

[Ref1][Ref2]

Form Management approach
Minor (trait)
  • Folic acid supplementation (to support red cell production) – all patients
  • Hydroxyurea (to induce fetal haemoglobin production) – in selected patients
  • Occasional red cell transfusion during specific circumstances (e.g. acute infection, pregnancy, surgery) (regular transfusions is typically not necessary)
Major
  • Mainstay of management is regular red cell transfusion
  • Curative treatment options

Conditional Management

[Ref]

Management Description / notes
Splenectomy Primary indication: symptomatic splenomegaly
Curative treatment
  • Allogenic haematopoietic stem cell transplantation
  • Gene therapy

Iron Overload

Aetiology

Iron overload is a major complication of symptomatic alpha thalassaemia (esp. HbH disease), it can occur from 2 mechanisms:

  • Regular red cell transfusions (not typically needed in alpha thalassaemia)
  • Increased GI iron absorption (due to ineffective erythropoiesis) – main mechanism in non-transfusion dependent thalassaemia (esp. HbH disease)

Iron overload is an important and problematic complication as iron homeostasis is regulated by absorption, not excretion. The body has no active mechanism to remove excess iron.

The body stores excess iron as ferritin / haemosiderin. Iron loss only occurs passively (without regulation) via shedding of skin cells, sloughing of gut mucosa, menstruation and minor blood loss.

Clinical Manifestation

Affected organ(s) Clinical manifestation
Systemic / general
  • Fatigue
  • Weakness
  • Malaise
Joints
  • Arthralgia (esp. 2nd and 3rd MCP joints) → painful handshake sign
  • Pseudogout (chondrocalcinosis)
  • Premature osteoarthritis
Skin
  • Bronze or slate-grey hyperpigmentation
Liver
  • Hepatomegaly
  • RUQ pain / discomfort
  • Cirrhosis
  • HCC (major cause of death)
Heart
  • Dilated / restrictive cardiomyopathy
  • Arrhythmias (e.g. atrial fibrillation) / conduction abnormalities
Endocrine organs
  • Pituitary gland → hypopituitarism (hypogonadotropic hypogonadism → delayed puberty, infertility, amenorrhoea)
  • Thyroid → hypothyroidism
  • Parathyroid → hypocalcaemia
  • Pancreas → late-onset diabetes

Detection and Diagnosis

[Ref]

  • Gold standard: MRI (measures liver and cardiac iron levels)
  • Serum ferritin level (less precise than MRI, used for routine serial monitoring to track trends)

Management

Management is with iron chelation therapy (agents that bind to excess iron and allow active excretion in urine and/or faeces).

General indications: [Ref]

  • Transfusion-dependent thalassaemias
    • Hb Bart’s hydrops fetalis
    • Beta thalassaemia major
  • Non-transfusion-dependent thalassaemias with
    • ↑ Serum ferritin (>800 μ/L)
    • ↑ Liver iron concentration (>5 mg/g dry weight)

Key iron chelating agents: [Ref]

  • Deferoxamine (subcutaneous / IV)
  • Deferasirox (oral)
  • Deferiprone (oral) – often used as 2nd line

Note that the management of iron overload (i.e. secondary haemochromatosis) is different to those of primary (genetic) haemochromatosis, where 1st line is regular venesection and 2nd line is iron chelation therapy.

Share Your Feedback Below

UK medical guidelines made easy. From guidelines to genius in minutes!

Quick Links

Cookie Policy

Social Media

© 2026 GUIDELINE GENIUS LTD