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Hylolymphemia
Hypolymphemia
Leukaemoid reaction lymphocytic
Lymphocytic leukopenia
Lymphocytopenia
Lymphopenia
Monocytic
Myelocytic
Sublymphemia

Translation of "lymphopenia " (English → French) :



lymphopenia | hylolymphemia | lymphocytic leukopenia | lymphocytopenia | sublymphemia

lymphopénie
médecine > vénéréologie
médecine > vénéréologie


An extremely rare association syndrome, described in only two brothers to date (one of which died at 2 months of age), characterised by aplasia cutis congenita of the vertex and generalised oedema (as well as hypoproteinaemia and lymphopenia) due to

syndrome d'aplasie cutanée congénitale-lymphangiectasie intestinale
SNOMEDCT-BE (one of which died at 2 months of age), characterised by aplasia cutis congenita of the vertex and generalised oedema (as well as hypoproteinaemia and lymphopenia) due to / 720500008
SNOMEDCT-BE (disorder) / 720500008


An extremely rare association syndrome, described in only two brothers to date (one of which died at 2 months of age), characterized by aplasia cutis congenita of the vertex and generalized edema (as well as hypoproteinemia and lymphopenia) due to in

aplasie cutanée congénitale autosomique récessive
SNOMEDCT-BE (one of which died at 2 months of age), characterised by aplasia cutis congenita of the vertex and generalised oedema (as well as hypoproteinaemia and lymphopenia) due to / 720500008
SNOMEDCT-BE (disorder) / 720500008


lymphocytopenia [ lymphopenia | sublymphemia | hypolymphemia ]

lymphocytopénie [ lymphopénie ]
Lymphatic System | Symptoms (Medicine)
Système lymphatique | Symptômes (Médecine)


lymphocytopenia | lymphopenia

lymphocytopénie | lymphopénie
IATE - Health
IATE - Health


Leukaemoid reaction:lymphocytic | monocytic | myelocytic | Leukocytosis Lymphocytosis (symptomatic) Lymphopenia Monocytosis (symptomatic) Plasmacytosis

Leucocytose Lymphocytose (symptomatique) Lymphopénie Monocytose (symptomatique) Plasmocytose Réaction leucémoïde de type:lymphocytaire | monocytaire | myélocytaire
WORLD HEALTH ORGANIZATION ICD-10: D72.8
WORLD HEALTH ORGANIZATION ICD-10: D72.8


A rare genetic primary immunodeficiency disorder with characteristics of profound circulating monocytopenia, B- and NK-cell lymphopenia and severe dendritic cell decrease, which manifests clinically with disseminated mycobacterial and viral infection

monocytopénie avec susceptibilité aux infections
SNOMEDCT-BE (disorder) / 778024005
SNOMEDCT-BE (disorder) / 778024005




Others have searched : leukaemoid reaction lymphocytic    hylolymphemia    hypolymphemia    lymphocytic leukopenia    lymphocytopenia    lymphopenia    monocytic    myelocytic    sublymphemia    


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'lymphopenia'

Date index:2022-10-26 -

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