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What is Agammaglobulinemia, non-Bruton type?

What is Agammaglobulinemia, non-Bruton type?

  • Agammaglobulinemia, non-Bruton type: An inherited immune system disorder involving a lack of mature B lymphocyte.

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

Agammaglobulinemia, non-Bruton type: Introduction

Types of Agammaglobulinemia, non-Bruton type:

Broader types of Agammaglobulinemia, non-Bruton type:

What causes Agammaglobulinemia, non-Bruton type?

Causes of Agammaglobulinemia, non-Bruton type: see causes of Agammaglobulinemia, non-Bruton type

What are the symptoms of Agammaglobulinemia, non-Bruton type?

Symptoms of Agammaglobulinemia, non-Bruton type: see symptoms of Agammaglobulinemia, non-Bruton type

Agammaglobulinemia, non-Bruton type: Testing

Diagnostic testing: see tests for Agammaglobulinemia, non-Bruton type.

Misdiagnosis: see misdiagnosis and Agammaglobulinemia, non-Bruton type.

How is it treated?

Doctors and Medical Specialists for Agammaglobulinemia, non-Bruton type: Medical Geneticist ; see also doctors and medical specialists for Agammaglobulinemia, non-Bruton type.
Treatments for Agammaglobulinemia, non-Bruton type: see treatments for Agammaglobulinemia, non-Bruton type

Name and Aliases of Agammaglobulinemia, non-Bruton type

Main name of condition: Agammaglobulinemia, non-Bruton type

Other names or spellings for Agammaglobulinemia, non-Bruton type:

Agammaglobulinemia due to early proB cell defect, Agammaglobulinemia, autosomal recessive

Agammaglobulinemia due to early proB cell defect, Agammaglobulinemia, autosomal recessive
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

 

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