Vertaling van "bruton's hypogammaglobulinemia " (Engels → Frans) :

Bruton's disease | Bruton's hypogammaglobulinemia | Bruton's X-linked agammaglobulinemia | X-linked agammaglobulinaemia | XLA [Abbr.]
maladie de Bruton

Bruton's agammaglobulinemia [ Bruton's disease | congenital hypogammaglobulinemia | Bruton hypogammaglobulinemia | X-linked hypogammaglobulinemia | Bruton type agammaglobulinemia | X-linked agammaglobulinemia ]
maladie de Bruton [ agammaglobulinémie liée au sexe | agammaglobulinémie liée à l'X | agammaglobulinémie de Bruton ]

congenital hypogammaglobulinaemia | congenital hypogammaglobulinemia
hypogammaglobulinémie congénitale

antibody deficiency syndrome | Bruton disease
syndrome par manque d'anticorps

Bruton's type agammaglobulinemia
agammaglobulinémie type Bruton

Autosomal recessive agammaglobulinaemia (Swiss type) X-linked agammaglobulinaemia [Bruton] (with growth hormone deficiency)
Agammaglobulinémie:autosomique récessive (type suisse) | liée au chromosome X [Bruton] (avec déficit de l'hormone de croissance)

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
syndrome de maladie veino-occlusive hépatique-immunodéficience

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
syndrome d'insuffisance antéhypophysaire-déficit immunitaire variable