FANCD1

Introduction: FANCD1

Description of FANCD1

FANCD1 (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 D1 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 D1:
  »Introduction: Fanconi's anemia - Complementation group D1
  »Symptoms of Fanconi's anemia - Complementation group D1
  »Treatments for Fanconi's anemia - Complementation group D1

FANCD1 as a Disease

FANCD1: Another name for Fanconi's anemia - Complementation group D1 (or close medical condition association).
  »Introduction: Fanconi's anemia - Complementation group D1
  »Symptoms of Fanconi's anemia - Complementation group D1
  »Treatments for Fanconi's anemia - Complementation group D1

Symptoms of FANCD1 (Fanconi's anemia - Complementation group D1)

Some of the symptoms of FANCD1 incude:

• Reduced number of blood platelets
• Reduced red blood cell count
• Reduced white blood cell count
• Pancytopenia
• Fatigue

See full list of 11 symptoms of FANCD1 (Fanconi's anemia - Complementation group D1)

Treatments for FANCD1 (Fanconi's anemia - Complementation group D1)

Treatments for FANCD1 (Fanconi's anemia - Complementation group D1) include:

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

Read more about treatments for FANCD1

Treatment of FANCD1: For more treatment information about FANCD1, see treatment of Fanconi's anemia - Complementation group D1 (FANCD1)

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