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Alcoholic hallucinosis
Chronic alcoholism Dipsomania Drug addiction
Delirium tremens
Depressive neurosis
Disorder of personality and behaviour
Jealousy
Neurotic depression Persistent anxiety depression
Paranoia
Personality disorder
Psychoactive substance abuse
Psychogenic depression
Psychosis NOS
Reactive depression
Single episodes of depressive reaction

Translation of "Severe " (English → French) :

A rare multiple malformation syndrome with characteristics of severe intrauterine growth retardation, severe microcephaly with a sloping forehead, severe ichthyosis (collodion baby type), and facial dysmorphism. Severe central nervous system defects

syndrome de Neu-Laxova
SNOMEDCT-BE (collodion baby type), and facial dysmorphism. Severe central nervous system defects / 77817004
SNOMEDCT-BE (disorder) / 77817004


Definition: In typical mild, moderate, or severe depressive episodes, the patient suffers from lowering of mood, reduction of energy, and decrease in activity. Capacity for enjoyment, interest, and concentration is reduced, and marked tiredness after even minimum effort is common. Sleep is usually disturbed and appetite diminished. Self-esteem and self-confidence are almost always reduced and, even in the mild form, some ideas of guilt or worthlessness are often present. The lowered mood varies little from day to day, is unresponsive to circumstances and may be accompanied by so-called somatic symptoms, such as loss of interest and pleas ...[+++]

Définition: Dans les épisodes typiques de chacun des trois degrés de dépression: léger, moyen ou sévère, le sujet présente un abaissement de l'humeur, une réduction de l'énergie et une diminution de l'activité. Il existe une altération de la capacité à éprouver du plaisir, une perte d'intérêt, une diminution de l'aptitude à se concentrer, associées couramment à une fatigue importante, même après un effort minime. On observe habituellement des troubles du sommeil, et une diminution de l'appétit. Il existe presque toujours une diminution de l'estime de soi et de la confiance en soi et, fréquemment, des idées de culpabilité ou de dévalorisation, même dans les formes légères. L'humeur dépressive ne varie guère d'un jour à l'autre ou selon les c ...[+++]
WORLD HEALTH ORGANIZATION ICD-10: F32
WORLD HEALTH ORGANIZATION ICD-10: F32


An X-linked disorder of purine metabolism comprised of two forms: an early-onset severe form with characteristics of gout, urolithiasis, and neurodevelopmental anomalies (severe PRPP synthetase superactivity) and a mild late-onset form with no neurol

hyperactivité de la phosphoribosylpyrophosphate synthétase
SNOMEDCT-BE (severe PRPP synthetase superactivity) and a mild late-onset form with no neurol / 723454008
SNOMEDCT-BE (disorder) / 723454008


A unique form of congenital adrenal hyperplasia characterised by glucocorticoid deficiency, severe sexual ambiguity in both sexes and skeletal (especially craniofacial) malformations. Prenatal androgen excess is responsible for severe virilisation of

hyperplasie congénitale des surrénales par déficit en cytochrome P450 oxydoréductase
SNOMEDCT-BE (especially craniofacial) malformations. Prenatal androgen excess is responsible for severe virilisation of / 715733000
SNOMEDCT-BE (disorder) / 715733000


A rare genetic neurodegenerative disorder with characteristics of severe, persistent hypotonia (presenting at birth or in early infancy), severe global developmental delay (with poor or absent speech, difficulty or inability to roll, sit or walk), pr

syndrome d'hypotonie-trouble sévère du langage-retard cognitif sévère
SNOMEDCT-BE (presenting at birth or in early infancy), severe global developmental delay (with poor or absent speech, difficulty or inability to roll, sit or walk), pr / 763722004
SNOMEDCT-BE (disorder) / 763722004


A rare mitochondrial substrate carrier disorder with characteristics of severe muscular hypotonia, seizures beginning in the first year of life and arrested psychomotor development (affecting mainly motor skills). Severe spasticity with hyperreflexia

encéphalopathie épileptique avec démyélinisation cérébrale généralisée
SNOMEDCT-BE (affecting mainly motor skills). Severe spasticity with hyperreflexia / 726702005
SNOMEDCT-BE (disorder) / 726702005


Definition: This category differs from others in that it includes disorders identifiable on the basis of not only symptoms and course but also the existence of one or other of two causative influences: an exceptionally stressful life event producing an acute stress reaction, or a significant life change leading to continued unpleasant circumstances that result in an adjustment disorder. Although less severe psychosocial stress ( life events ) may precipitate the onset or contribute to the presentation of a very wide range of disorders classified elsewhere in this chapter, its etiological importance is not always clear and in each case wi ...[+++]

Définition: Cette catégorie est différente des autres dans la mesure où sa Définition: ne repose pas exclusivement sur les symptomes et l'évolution, mais également sur l'un ou l'autre des deux facteurs étiologiques suivants: un événement particulièrement stressant entraînant une réaction aiguë à un facteur de stress, ou un changement particulièrement marquant dans la vie du sujet, comportant des conséquences désagréables et durables et aboutissant à un trouble de l'adaptation. Des facteurs de stress psychosociaux relativement peu sévères parmi les événements de la vie ( life events ) peuvent précipiter la survenue ou influencer le tablea ...[+++]
WORLD HEALTH ORGANIZATION ICD-10: F43
WORLD HEALTH ORGANIZATION ICD-10: F43


Definition: A chronic depression of mood, lasting at least several years, which is not sufficiently severe, or in which individual episodes are not sufficiently prolonged, to justify a diagnosis of severe, moderate, or mild recurrent depressive disorder (F33.-). | Depressive:neurosis | personality disorder | Neurotic depression Persistent anxiety depression

Définition: Abaissement chronique de l'humeur, persistant au moins plusieurs années, mais dont la sévérité est insuffisante, ou dont la durée des différents épisodes est trop brève, pour justifier un diagnostic de trouble dépressif récurrent, sévère, moyen ou léger (F33.-). | Dépression:anxieuse persistante | névrotique | Névrose | Personnalité | dépressive
WORLD HEALTH ORGANIZATION ICD-10: F34.1
WORLD HEALTH ORGANIZATION ICD-10: F34.1


Definition: This block contains a wide variety of disorders that differ in severity and clinical form but that are all attributable to the use of one or more psychoactive substances, which may or may not have been medically prescribed. The third character of the code identifies the substance involved, and the fourth character specifies the clinical state. The codes should be used, as required, for each substance specified, but it should be noted that not all fourth character codes are applicable to all substances. Identification of the psychoactive substance should be based on as many sources of information as possible. These include sel ...[+++]

Modificateurs Les subdivisions suivantes peuvent être utilisées comme quatrième chiffre avec les rubriques F10-F19: Code Titre .0 Intoxication aiguë Etat consécutif à la prise d'une substance psycho-active et entraînant des perturbations de la conscience, des facultés cognitives, de la perception, de l'affect ou du comportement, ou d'autres fonctions et réponses psychophysiologiques. Les perturbations sont directement liées aux effets pharmacologiques aigus de la substance consommée, et disparaissent avec le temps, avec guérison complète, sauf dans les cas ayant entraîné des lésions organiques ou d'autres complications. Parmi les complic ...[+++]
WORLD HEALTH ORGANIZATION ICD-10: F10-F19
WORLD HEALTH ORGANIZATION ICD-10: F10-F19


A unique form of congenital adrenal hyperplasia characterized by glucocorticoid deficiency, severe sexual ambiguity in both sexes and skeletal (especially craniofacial) malformations. Prenatal androgen excess is responsible for severe virilization of

déficit en POR
SNOMEDCT-BE (especially craniofacial) malformations. Prenatal androgen excess is responsible for severe virilisation of / 715733000
SNOMEDCT-BE (disorder) / 715733000




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'Severe'

Date index:2024-03-21 -

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