Hyper-IgM syndrome type 3
Hyper-IgM syndrome type 3 is a rare immunodeficiency disorder characterized by a defective immune system that primarily affects males. The condition is caused by mutations in the CD40 ligand gene, which is involved in the activation of B cells and their subsequent transformation into plasma cells that produce antibodies.
Symptoms[edit | edit source]
The symptoms of Hyper-IgM syndrome type 3 typically begin in infancy or early childhood. They include frequent and severe bacterial infections, pneumonia, sinusitis, and meningitis. Other symptoms may include diarrhea, skin rashes, and liver disease.
Causes[edit | edit source]
Hyper-IgM syndrome type 3 is caused by mutations in the CD40 ligand gene. This gene provides instructions for making a protein that is essential for the activation of B cells, which are a type of white blood cell that produces antibodies. When the CD40 ligand protein is defective, B cells cannot transform into plasma cells to produce antibodies, leading to an impaired immune response.
Diagnosis[edit | edit source]
The diagnosis of Hyper-IgM syndrome type 3 is based on the presence of characteristic symptoms, a detailed patient history, a thorough clinical evaluation, and specialized tests. These tests may include measuring the levels of different types of antibodies in the blood and genetic testing to identify mutations in the CD40 ligand gene.
Treatment[edit | edit source]
There is currently no cure for Hyper-IgM syndrome type 3. Treatment is aimed at managing symptoms and preventing infections. This may include antibiotics to treat bacterial infections, immunoglobulin therapy to boost the immune system, and in severe cases, a bone marrow transplant.
Prognosis[edit | edit source]
The prognosis for individuals with Hyper-IgM syndrome type 3 varies. Some individuals have a normal lifespan with proper management, while others may have a shortened lifespan due to severe recurrent infections and complications such as liver disease.
See also[edit | edit source]
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