Vertaling van "Hypogammaglobulinaemia syndrome " (Engels → Nederlands) :

hypogammaglobulinaemia syndrome
hypogammaglobulinemie

congenital hypogammaglobulinaemia | congenital hypogammaglobulinemia
congenitale hypogammaglobulinemie

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
congenitale chronische diarree met proteïneverliezende enteropathie

Hereditary hypogammaglobulinaemia
hereditaire hypogammaglobulinemie

Agammaglobulinaemia with immunoglobulin-bearing B-lymphocytes Common variable agammaglobulinaemia [CVAgamma] Hypogammaglobulinaemia NOS
agammaglobulinemie met immunoglobulinedragende B-lymfocyten | 'common variable'-agammaglobulinemie [CVA-gamma] | hypogammaglobulinemie NNO

Nonfamilial hypogammaglobulinaemia
niet-familiale hypogammaglobulinemie

fragile x chromosome syndrome | fragile X syndrome | Fra-X syndrome | FRAXA syndrome | Martin-Bell syndrome | FRAX [Abbr.] | FXS [Abbr.]
fragiel-X-syndroom | FXS [Abbr.]

A group of dysmorphic complexes (including Charlie M syndrome, Hanhart syndrome and glossopalatine ankylosis) with the association of severe asymmetric limb defects (primarily involving distal segments) and abnormalities of the oral cavity and mandib
syndroom van Möbius

A rare malignant hematologic disease characterized by clonal proliferation of myeloid blasts, primarily involving the bone marrow, in association with congenital disorders (e.g. Fanconi anemia, dyskeratosis congenita, Bloom syndrome, Down syndrome, c
overgeërfde acute myeloïde leukemie

syndrome
syndroom | ziektebeeld