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Bright's disease
Brightism
Briquet's disorder Multiple psychosomatic disorder
Chronic Bright's disease
Chronic diffuse glomerulonephritis
Chronic familial erythremia
Chronic glomerular disease
Chronic glomerulonephritis
Chronic lobular glomerulonephritis
Chronic membranous glomerulonephritis
Chronic nephritis
Chronic primary glomerulonephritis
Chronic uraemia diffuse sclerosing glomerulonephritis
Cooley's anemia
Cooley's syndrome
Cooley's-disease
Cooley-Lee syndrome
Dameshek's syndrome
Erythroblastic anemia
Glomerulonephritis
Hereditary leptocytosis
Hypocomplementemic glomerulonephritis
Lobular glomerulonephritis
MPGN
Mediterranean anemia
Mediterranean disease
Membranoproliferative glomerulonephritis
Mesangiocapillary glomerulonephritis
Nephritis
Primary erythroblastic anemia
Renal disease NOS
Secondary small white kidney
Target cell anemia
Target-oval cell syndrome
Thalassaemia major
Thalassemia major
Thalassemic syndrome

Traduction de «chronic primary glomerulonephritis » (Anglais → Français) :

chronic primary glomerulonephritis

glomérulonéphrite chronique primitive


chronic glomerulonephritis | chronic Bright's disease | chronic nephritis | Bright's disease | brightism | chronic diffuse glomerulonephritis | secondary small white kidney

glomerulonéphrite chronique | néphrite chronique | brightisme | maladie de Bright | mal de Bright


chronic lobular glomerulonephritis | hypocomplementemic glomerulonephritis | lobular glomerulonephritis | membranoproliferative glomerulonephritis | mesangiocapillary glomerulonephritis | MPGN [Abbr.]

glomérulonéphrite membrano-proliférative


chronic membranous glomerulonephritis

glomérulo-néphrite chronique membraneuse


chronic:glomerular disease | glomerulonephritis | nephritis | renal disease NOS

glomérulonéphrite | glomérulopathie | maladie rénale SAI | néphrite | néphropathie | chronique


chronic uraemia diffuse sclerosing glomerulonephritis

glomérulonéphrite sclérosante diffuse urémie chronique


Cooley's anemia | Cooley's-disease | Cooley's syndrome | Cooley-Lee syndrome | Dameshek's syndrome | chronic familial erythremia | erythroblastic anemia | hereditary leptocytosis | Mediterranean anemia | Mediterranean disease | primary erythroblastic anemia | target cell anemia | target-oval cell syndrome | thalassaemia major | thalassemia major | thalassemic syndrome

maladie de Cooley | anémie de Cooley | anémie érythroblastique familiale primitive | anémie méditerranéenne | anémie microcytaire familiale | érythrémie chronique familiale | hémo-ostéopathie de Cooley | leptocytose héréditaire | maladie méditerranéenne | syndrome de Cooley-Lee | thalassanémie | thalassémie érythroblastique familiale génotypique | thalassémie majeure | anémie érythrémique


Definition: The main features are multiple, recurrent and frequently changing physical symptoms of at least two years' duration. Most patients have a long and complicated history of contact with both primary and specialist medical care services, during which many negative investigations or fruitless exploratory operations may have been carried out. Symptoms may be referred to any part or system of the body. The course of the disorder is chronic and fluctuating, and is often associated with disruption of social, interpersonal, and fami ...[+++]

Définition: Les principales caractéristiques sont des symptômes physiques multiples, récurrents et variables dans le temps, persistant au moins deux ans. Dans la plupart des cas, les sujets entretiennent, depuis longtemps, des relations complexes avec les services médicaux, spécialisés et non spécialisés, et ont subi de nombreuses investigations ou interventions exploratrices négatives. Les symptômes peuvent renvoyer à n'importe quel système ou partie du corps. Le trouble a une évolution chronique et fluctuante, et s'accompagne souvent d'une altération du comportement social, interpersonnel et familial. Quand le trouble est de durée plus ...[+++]


An extremely rare genetic endocrine disease with characteristics of primary adrenal insufficiency, dystrophic myopathy, hepatic steatosis, severe psychomotor delay, megalocornea, failure to thrive, chronic constipation, and terminal bladder ectasia w

adrénomyodystrophie


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