A rare genetic intestinal disease characterised by early-onset chronic non-infectious, non-bloody, watery diarrhoea associated with protein-losing enteropathy, which results in hypoalbuminaemia, hypogammaglobulinaemia and elevated stool alpha-1-antit

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diarrhée chronique congénitale avec entéropathie exsudative

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Nonfamilial hypogammaglobulinaemia

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Hypogammaglobulinémie non familiale

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Agammaglobulinaemia with immunoglobulin-bearing B-lymphocytes Common variable agammaglobulinaemia [CVAgamma] Hypogammaglobulinaemia NOS

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Agammaglobulinémie:avec lymphocytes B porteurs d'immunoglobulines | commune variable | Hypogammaglobulinémie SAI

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Hereditary hypogammaglobulinaemia

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Hypogammaglobulinémie héréditaire

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TRADUCTIONS EN CONTEXTE

Human normal immunoglobulin (ivig) || Kiovig || 2011 || Extension of indication to include treatment of multifocal motor neuropathy and hypogammaglobulinaemia in patients after allogeneic haematopoietic stem cell transplantation in adults and children

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Immunoglobuline humaine normale (ivig) || Kiovig || 2011 || Extension de l’indication pour inclure le traitement de la neuropathie motrice multifocale et hypogammaglobulinémie après une greffe de cellules souches hématopoïétiques allogéniques chez les adultes et les enfants

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Date index: 2022-01-31