Abstract
B-cell linker (BLNK) protein is a non-redundant adaptor molecule in the signaling pathway activated by (pre) B-cell antigen receptor signals. We present two siblings with a homozygous deleterious frameshift mutation in BLNK, resulting in a block of B cell development in the bone marrow at the preB1 to preB2 stage, absence of circulating B cells and agammaglobulinemia. This is the first description of an enteroviral infection associated arthritis and dermatitis in a patient with BLNK deficiency.
MeSH terms
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Adaptor Proteins, Signal Transducing / deficiency*
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Adaptor Proteins, Signal Transducing / genetics
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Agammaglobulinemia / complications*
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Agammaglobulinemia / congenital*
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Agammaglobulinemia / diagnosis
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Agammaglobulinemia / drug therapy
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Arthritis / diagnosis
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Arthritis / etiology
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B-Lymphocytes / immunology
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B-Lymphocytes / metabolism
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Child
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Consanguinity
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DNA Mutational Analysis
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Dermatitis / diagnosis
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Dermatitis / etiology
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Enterovirus Infections / diagnosis
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Enterovirus Infections / etiology*
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Homozygote
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Humans
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Immunophenotyping
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Male
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Mutation
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Phenotype
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Siblings
Substances
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Adaptor Proteins, Signal Transducing
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B cell linker protein