Autosomal recessive agammaglobulinaemia (Swiss type) X-linked agammaglobulinaemia [Bruton] (with growth hormone deficiency)

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Agammaglobulinémie:autosomique récessive (type suisse) | liée au chromosome X [Bruton] (avec déficit de l'hormone de croissance)

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Syndrome that is characterized by the association of severe hypogammaglobulinemia, combined T and B cell immunodeficiency, absent lymph node germinal centers, absent tissue plasma cells and hepatic veno-occlusive disease. Mutations in the gene coding

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syndrome de maladie veino-occlusive hépatique-immunodéficience

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A rare genetic endocrine disease characterized by the association of common variable immunodeficiency manifesting with hypogammaglobulinemia and recurrent or severe childhood-onset sinopulmonary infections, followed, possibly many years later, by sym

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syndrome d'insuffisance antéhypophysaire-déficit immunitaire variable

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Others have searched : bruton bruton disease bruton type agammaglobulinemia bruton's x-linked agammaglobulinemia bruton's agammaglobulinemia bruton's disease bruton's type agammaglobulinemia x-linked agammaglobulinaemia x-linked agammaglobulinemia antibody deficiency syndrome Bruton's hypogammaglobulinemia

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Date index: 2023-09-09