Autosomal agammaglobulinemia
Autosomal agammaglobulinemia: Agammaglobulinemia, non-Bruton type (autosomal agammaglobulinemia) is a rare form of agammaglobulinemia, a primary immunodeficiency disease, and is characterized by variable immune dysfunction with frequent and recurrent bacterial infections and/or chronic diarrhea.
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Symptoms List: Autosomal agammaglobulinemia
Symptoms and clinical features may include:2 Clinical Features of Autosomal agammaglobulinemia:
- High palate
- Sinusitis
- Epicanthus
- Hypertelorism
- Chronic otitis media
- Conjunctivitis
- Skin rash
- Meningitis
- Arthritis
- Failure to thrive
- Recurrent skin infections
- Neutropenia
- Dehydration
- Fever
- Diarrhea
- Malabsorption
- Bronchiectasis
- Recurrent respiratory infections
- Immunodeficiency
- Osteomyelitis
- Agammaglobulinemia
- External ear malformation
- Hepatitis ...
Types of Autosomal agammaglobulinemia
Some types of this condition may include:3 Types of Autosomal agammaglobulinemia:
- Agammaglobulinemia 2, Autosomal Recessive
- Agammaglobulinemia 3, Autosomal Recessive
- Agammaglobulinemia 4, Autosomal Recessive
- Agammaglobulinemia 5, Autosomal Dominant
- Agammaglobulinemia 6, Autosomal Recessive
- Agammaglobulinemia 7, Autosomal Recessive
Causes
See also causal information:
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References
- Source: Monarch Initiative
- Source: Human Phenotype Ontology
- Source: NCI Thesaurus
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Note: This site is for informational purposes only and is not medical advice. See your doctor or other qualified medical professional for all your medical needs.