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FANCD2

Introduction: FANCD2

Description of FANCD2

FANCD2 (medical condition): Fanconi's anemia is a rare inherited blood disorder characterized by the inability of the bone marrow to produce blood cells. The subtype called Complementation group D2 refers to a genetic subtype of the disease. An increased incidence of leukemias and other cancers is associated with this condition and various skeletal abnormalities and other birth defects may also be present. The condition is present at birth but symptoms of the blood problems are often not evident until later in childhood - in rare cases, the condition may not be diagnosed until adulthood.

See also:

Fanconi's anemia - Complementation group D2:
  »Introduction: Fanconi's anemia - Complementation group D2
  »Symptoms of Fanconi's anemia - Complementation group D2
  »Treatments for Fanconi's anemia - Complementation group D2

FANCD2 as a Disease

FANCD2: Another name for Fanconi's anemia - Complementation group D2 (or close medical condition association).
  »Introduction: Fanconi's anemia - Complementation group D2
  »Symptoms of Fanconi's anemia - Complementation group D2
  »Treatments for Fanconi's anemia - Complementation group D2

Symptoms of FANCD2 (Fanconi's anemia - Complementation group D2)

Some of the symptoms of FANCD2 incude:

See full list of 11 symptoms of FANCD2 (Fanconi's anemia - Complementation group D2)

Treatments for FANCD2 (Fanconi's anemia - Complementation group D2)

Treatments for FANCD2 (Fanconi's anemia - Complementation group D2) include:

  • Drug therapy - androgens, hematopoietic (blood-stimulating) growth factors; blood transfusions, bone marrow transplant.

Read more about treatments for FANCD2

Treatment of FANCD2: For more treatment information about FANCD2, see treatment of Fanconi's anemia - Complementation group D2 (FANCD2)

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