Vertaling van "congenital hypogammaglobulinaemia " (Engels → Nederlands) :

congenital hypogammaglobulinaemia | congenital hypogammaglobulinemia
congenitale hypogammaglobulinemie

birth defect | congenital anomaly | congenital defect | congenital disease | congenital disorder | congenital malformation
aangeboren aandoening

congenital disease [ congenital deformity | congenital malformation ]
aangeboren ziekte [ aangeboren afwijking ]

hypogammaglobulinaemia syndrome
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

Nonfamilial hypogammaglobulinaemia
niet-familiale 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

Hereditary hypogammaglobulinaemia
hereditaire hypogammaglobulinemie

Belongs to the group of multiple congenital anomalies/mental retardation syndromes with intellectual deficit, distinctive facies (upward slanting palpebral fissures, squint), kyphoscoliosis, diastasis recti, cryptorchidism, and a congenital heart def
syndroom van McDonough

Idiopathic congenital hypothyroidism is a type of primary congenital hypothyroidism whose cause and prevalence are unknown. Clinical manifestations are those of other forms of congenital hypothyroidism. Goiter is always absent. Ultrasound examination
idiopathische congenitale hypothyreoïdie