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Dictionary » Reticular dysgenesia
 

Reticular dysgenesia

Introduction: Reticular dysgenesia

Description of Reticular dysgenesia

Reticular dysgenesia (medical condition): A rare condition characterized by the defective development of T-cells, B...more »

See also:

De Vaal syndrome:
  »Introduction: De Vaal syndrome
  »Symptoms of De Vaal syndrome

Reticular dysgenesia: Related Topics

These medical condition or symptom topics may be relevant to medical information for Reticular dysgenesia:

Reticular dysgenesia: Rare Disease

Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

Reticular dysgenesia is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Reticular dysgenesia, or a subtype of Reticular dysgenesia, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Reticular dysgenesia as a Disease

Reticular dysgenesia: Another name for De Vaal syndrome (or close medical condition association).
  »Introduction: De Vaal syndrome
  »Symptoms of De Vaal syndrome

Reticular dysgenesia: Related Diseases

Reticular dysgenesia: Reticular dysgenesia is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of Reticular dysgenesia (De Vaal syndrome)

Some of the symptoms of Reticular dysgenesia incude:

  • Severe infection following birth
  • Severely impaired development
  • Enlarged lymph nodes
  • Focal tissue necrosis
  • Reduced level of lymphocytes

Reticular dysgenesia: Related Disease Topics

These medical disease topics may be related to Reticular dysgenesia:

Terms associated with Reticular dysgenesia:

Terms Similar to Reticular dysgenesia:

Source - NIH

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