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Coronavirus lié au syndrome respiratoire aigu sévère
Syndrome d'Alport lié à l'X-léiomyomatose diffuse
Syndrome d'anomalie des cônes avec myopie lié à l'X
Syndrome lié au lupus érythémateux systémique
Syndrome lymphoprolifératif auto-immun
Syndrome neurodégénératif lié à l'X type Bertini

Translation of "syndrome lymphoprolifératif lié à l x " (French → English) :

TERMINOLOGY
see also In-Context Translations below
syndrome lymphoprolifératif auto-immun

Autoimmune lymphoproliferative syndrome
SNOMEDCT-BE (disorder) / 702444009
SNOMEDCT-BE (disorder) / 702444009


syndrome lymphoprolifératif auto-immun avec infections virales récurrentes

A rare genetic disorder with characteristics of lymphadenopathy and/or splenomegaly and recurrent infections due to herpes viruses. Prevalence of this disorder is not known. It is extremely rare with four individuals in one family identified to date.
SNOMEDCT-BE (disorder) / 722290008
SNOMEDCT-BE (disorder) / 722290008


leucémie aigüe myéloïde et syndromes myélodysplasiques liés aux inhibiteurs de la topoisomérase II

A subgroup of therapy-related myeloid neoplasms (t-MN), associated with treatment of an unrelated neoplastic disease with cytotoxic agents, like etoposide, doxorubicin, daunorubicin and others. The neoplastic cells often show rearrangements involving
SNOMEDCT-BE (disorder) / 766046007
SNOMEDCT-BE (t-MN), associated with treatment of an unrelated neoplastic disease with cytotoxic agents, like etoposide, doxorubicin, daunorubicin and others. The neoplastic cells often show rearrangements involving / 766046007


syndrome neurodégénératif lié à l'X type Bertini

This syndrome is characterised by generalised hypotonia, psychomotor deficit, congenital ataxia and recurrent bronchopulmonary infections. It has been described in seven males from three generations of a family. Five of them died during the first yea
SNOMEDCT-BE (disorder) / 718849008
SNOMEDCT-BE (disorder) / 718849008


leucémie aigüe myéloïde et syndromes myélodysplasiques liés aux agents alkylants

A subgroup of therapy-related myeloid neoplasms (t-MN), associated with a treatment of an unrelated neoplastic or autoimmune disease with cytotoxic agents, like cyclophosphamid, platins, melphalan and others. The neoplastic cells typically harbor unb
SNOMEDCT-BE (disorder) / 766045006
SNOMEDCT-BE (t-MN), associated with a treatment of an unrelated neoplastic or autoimmune disease with cytotoxic agents, like cyclophosphamid, platins, melphalan and others. The neoplastic cells typically harbor unb / 766045006


leucémie aigüe myéloïde et syndromes myélodysplasiques liés aux radiations

A subgroup of therapy-related myeloid neoplasms (t-MN), associated with treatment of an unrelated neoplastic disease with radiation. The neoplastic cells typically harbor unbalanced aberrations of chromosomes 5 and 7 (monosomy 5/del(5q) and monosomy
SNOMEDCT-BE (disorder) / 766048008
SNOMEDCT-BE (t-MN), associated with treatment of an unrelated neoplastic disease with radiation. The neoplastic cells typically harbor unbalanced aberrations of chromosomes 5 and 7 (monosomy 5/del(5q) and monosomy / 766048008


syndrome lié au lupus érythémateux systémique

Systemic lupus erythematosus-related syndrome
SNOMEDCT-BE (disorder) / 397856003
SNOMEDCT-BE (disorder) / 397856003


coronavirus lié au syndrome respiratoire aigu sévère

SARS-CoV
SNOMEDCT-BE (organism) / 415360003
SNOMEDCT-BE (organism) / 415360003


syndrome d'anomalie des cônes avec myopie lié à l'X

Bornholm eye disease
SNOMEDCT-BE (disorder) / 718718009
SNOMEDCT-BE (disorder) / 718718009


syndrome d'Alport lié à l'X-léiomyomatose diffuse

The association of X-linked Alport syndrome with leiomyomatosis of the oesophagus, tracheobronchial tree or female genitals has been reported in more than 30 families. The disease is due to a deletion involving the 5' terminal region of both COL4A5 a
SNOMEDCT-BE (disorder) / 726106004
SNOMEDCT-BE (disorder) / 726106004
IN-CONTEXT TRANSLATIONS
Les enfants atteints du syndrome lymphoprolifératif lié au chromosome X risquent davantage d'être atteints du LNH.

Children with X-linked lymphoproliferative syndrome have an increased risk of NHL.


Le syndrome lymphoprolifératif lié au chromosome X est une maladie héréditaire très rare au cours de laquelle les enfants développent une mononucléose infectieuse très grave due à une infection au virus Epstein-Barr.

X-linked lymphoproliferative disorder is a very rare inherited condition in which children develop very serious infectious mononucleosis because of infection with the Epstein-Barr virus.


Le syndrome lymphoprolifératif lié au chromosome X est une maladie héréditaire très rare au cours de laquelle les enfants développent une mononucléose infectieuse très grave due à une infection au virus Epstein-Barr.

X-linked lymphoproliferative disorder is a very rare inherited condition in which children develop very serious infectious mononucleosis because of infection with the Epstein-Barr virus.


Le syndrome lymphoprolifératif lié au chromosome X est un trouble rare qui provoque une réaction immunitaire déficiente face à une infection au virus d'Epstein-Barr.

X-linked lymphoproliferative syndrome is a rare condition that causes a defective immune response to infection with the Epstein-Barr virus.


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Le syndrome lymphoprolifératif lié au chromosome X est un trouble rare qui provoque une réaction immunitaire déficiente face à une infection au virus d'Epstein-Barr.

X-linked lymphoproliferative syndrome is a rare condition that causes a defective immune response to infection with the Epstein-Barr virus.


Le syndrome lymphoprolifératif lié au chromosome X est un trouble rare qui provoque une réaction immunitaire déficiente face à une infection au virus d'Epstein-Barr.

X-linked lymphoproliferative syndrome is a rare condition that causes a defective immune response to infection with the Epstein-Barr virus.


Les enfants atteints du syndrome lymphoprolifératif lié au chromosome X risquent davantage d'être atteints du LNH.

Children with X-linked lymphoproliferative syndrome have an increased risk of NHL.


Association à évaluer avec attention : Ciclosporine, tacrolimus : immunodépression excessive avec risque de syndrome lymphoprolifératif.

Concomitant use to assess carefully: Ciclosporine, tacrolimus: Excessive immunosuppression with risk of lymphoproliferative disease.


Tableau 2 : Effets indésirables survenus sous Rilonacept Regeneron chez des patients atteints d'un syndrome périodique lié à la cryopyrine

Table 2: Adverse reactions with Rilonacept Regeneron in CAPS patients


Chez les patients présentant un syndrome périodique lié à la cryopyrine, l’organisme produit des quantités excessives d’IL-1 bêta, ce qui peut entraîner des symptômes tels qu’une fièvre, un mal de tête, une fatigue, une éruption cutanée ou des douleurs au niveau des articulations ou des muscles.

In patients with CAPS, the body produces excessive amounts of IL-1 beta. This may lead to symptoms such as fever, headache, fatigue, skin rash, or painful joints and muscles.




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syndrome lymphoprolifératif lié à l x

Date index:2023-01-05 -

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