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Agammaglobulinemia, alymphocytotic type

Agammaglobulinemia, alymphocytotic type: Introduction

Agammaglobulinemia, alymphocytotic type: A rare inherited immunodeficiency disorder involving a lack of T and B lymphocytes which makes the patient susceptible to bacterial and viral infections. More detailed information about the symptoms, causes, and treatments of Agammaglobulinemia, alymphocytotic type is available below.

Symptoms of Agammaglobulinemia, alymphocytotic type

Treatments for Agammaglobulinemia, alymphocytotic type

Home Diagnostic Testing

Home medical testing related to Agammaglobulinemia, alymphocytotic type:

Wrongly Diagnosed with Agammaglobulinemia, alymphocytotic type?

Causes of Agammaglobulinemia, alymphocytotic type

Read more about causes of Agammaglobulinemia, alymphocytotic type.

Misdiagnosis and Agammaglobulinemia, alymphocytotic type

Unnecessary hysterectomies due to undiagnosed bleeding disorder in women: The bleeding disorder called Von Willebrand's disease is quite common in women, but often fails to be...read more »

Agammaglobulinemia, alymphocytotic type: Research Doctors & Specialists

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Evidence Based Medicine Research for Agammaglobulinemia, alymphocytotic type

Medical research articles related to Agammaglobulinemia, alymphocytotic type include:

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Agammaglobulinemia, alymphocytotic type: Animations

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Agammaglobulinemia, alymphocytotic type: Broader Related Topics

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Definitions of Agammaglobulinemia, alymphocytotic type:

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Agammaglobulinemia, alymphocytotic type as a "rare disease".
Source - Orphanet

Related Agammaglobulinemia, alymphocytotic type Info

More information about Agammaglobulinemia, alymphocytotic type

  1. Agammaglobulinemia, alymphocytotic type: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
 

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