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X-Linked Agammaglobulinemia
Introduction: X-Linked Agammaglobulinemia
X-Linked Agammaglobulinemia: XLA is sometimes called Bruton type, X-linked infantile, or congenital agammaglobulinemia. One out of 100,000 people have XLA. Defects on the X ... more about X-Linked Agammaglobulinemia.
X-Linked Agammaglobulinemia: Immune deficiency from lack of antibodies. More detailed information about the symptoms, causes, and treatments of X-Linked Agammaglobulinemia is available below.
Symptoms of X-Linked Agammaglobulinemia
See full list of 15 symptoms of X-Linked Agammaglobulinemia
Medical Textbooks Online about X-Linked Agammaglobulinemia
Free access (no registration).
Book excerpts: Copyright © 2008 Lippincott Williams & Wilkins. All rights reserved.
Less Common Symptoms of X-Linked Agammaglobulinemia
Read more about symptoms of X-Linked Agammaglobulinemia
Diagnostic Tests for X-Linked Agammaglobulinemia
- Immune function blood tests
- B-cell level blood test
- Immunoglobulin levels blood test
- Antibody tests - antibodies to specific germs are missing.
Read more about tests for X-Linked Agammaglobulinemia
Wrongly Diagnosed with X-Linked Agammaglobulinemia?
Causes of X-Linked Agammaglobulinemia
Read more about causes of X-Linked Agammaglobulinemia.
Treatments for X-Linked Agammaglobulinemia
- Intravenous immunoglobulin (IVIG) - a life-long course of treatment.
- PEG-ADA enzyme replacement therapy - for SCID with ADA deficiency.
Read more about treatments for X-Linked Agammaglobulinemia
Videos for X-Linked Agammaglobulinemia
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Statistics for X-Linked Agammaglobulinemia
- Medical statistics for X-Linked Agammaglobulinemia
- Prevalence and incidence statistics for X-Linked Agammaglobulinemia
- Death and Mortality statistics for X-Linked Agammaglobulinemia
- Society statistics for X-Linked Agammaglobulinemia
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Article Excerpts about X-Linked Agammaglobulinemia
XLA is sometimes called Bruton type, X-linked infantile, or congenital agammaglobulinemia. One out of 100,000 people have XLA. Defects on the X chromosome cause XLA. Only boys get XLA. That is because girls have two sets of X chromosomes, and the normal copy compensates for the faulty gene. (Source: excerpt from Primary Immune Deficiency, NIAID Fact Sheet: NIAID)
Definitions of X-Linked Agammaglobulinemia:
X-Linked Agammaglobulinemia is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that X-Linked Agammaglobulinemia, or a subtype of X-Linked Agammaglobulinemia,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
- X-Linked Agammaglobulinemia
- What is X-Linked Agammaglobulinemia?
- Online Medical Textbooks for X-Linked Agammaglobulinemia
- Prevalence and Incidence of X-Linked Agammaglobulinemia
- Videos related to X-Linked Agammaglobulinemia
- Causes of X-Linked Agammaglobulinemia
- Symptoms of X-Linked Agammaglobulinemia
- Diagnostic Tests for X-Linked Agammaglobulinemia
- Diagnosis of X-Linked Agammaglobulinemia
- Signs of X-Linked Agammaglobulinemia
- Complications of X-Linked Agammaglobulinemia
- Misdiagnosis of X-Linked Agammaglobulinemia
- Associated Conditions of X-Linked Agammaglobulinemia
- Inheritance and Genetics of X-Linked Agammaglobulinemia
- Treatments for X-Linked Agammaglobulinemia
- Doctors and Medical Specialists for X-Linked Agammaglobulinemia
- Statistics about X-Linked Agammaglobulinemia
- Statistics by Country for X-Linked Agammaglobulinemia
- Articles about X-Linked Agammaglobulinemia
- Glossary for X-Linked Agammaglobulinemia
- X-linked infantile hypogammaglobulinemia (Professional Guide to Diseases (Eighth Edition))
» Next page: What is X-Linked Agammaglobulinemia?
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