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Alcoholic hallucinosis
Arteriosclerotic dementia
Chronic alcoholism Dipsomania Drug addiction
Delirium tremens
Disorder of personality and behaviour
Jealousy
Paranoia
Paranoia Paranoid psychosis
Paraphrenia
Psychoactive substance abuse
Psychosis NOS
State
Traumatic neurosis

Translation of "usually small " (English → French) :

TERMINOLOGY
see also In-Context Translations below
Definition: Vascular dementia is the result of infarction of the brain due to vascular disease, including hypertensive cerebrovascular disease. The infarcts are usually small but cumulative in their effect. Onset is usually in later life. | arteriosclerotic dementia

Définition: La démence vasculaire résulte d'un infarcissement cérébral dû à une maladie vasculaire, par exemple, une maladie cérébrovasculaire hypertensive. Les infarctus sont habituellement de petite taille mais leurs effets sont cumulatifs. La démence survient habituellement à un âge avancé. | démence artériopathique
WORLD HEALTH ORGANIZATION ICD-10: F01
WORLD HEALTH ORGANIZATION ICD-10: F01


Definition: Arises as a delayed or protracted response to a stressful event or situation (of either brief or long duration) of an exceptionally threatening or catastrophic nature, which is likely to cause pervasive distress in almost anyone. Predisposing factors, such as personality traits (e.g. compulsive, asthenic) or previous history of neurotic illness, may lower the threshold for the development of the syndrome or aggravate its course, but they are neither necessary nor sufficient to explain its occurrence. Typical features include episodes of repeated reliving of the trauma in intrusive memories ( flashbacks ), dreams or nightmares, occurring against the persisting background of a sense of numbness and emotional blunting, detachment f ...[+++]

Définition: Ce trouble constitue une réponse différée ou prolongée à une situation ou à un événement stressant (de courte ou de longue durée), exceptionnellement menaçant ou catastrophique et qui provoquerait des symptômes évidents de détresse chez la plupart des individus. Des facteurs prédisposants, tels que certains traits de personnalité (par exemple compulsive, asthénique) ou des antécédents de type névrotique, peuvent favoriser la survenue du syndrome ou aggraver son évolution; ces facteurs ne sont pas toutefois nécessaires ou suffisants pour expliquer la survenue du syndrome. Les symptômes typiques comprennent la reviviscence répétée de l'événement traumatique, dans des souvenirs envahissants ( flashbacks ), des rêves ou des cauchem ...[+++]
WORLD HEALTH ORGANIZATION ICD-10: F43.1
WORLD HEALTH ORGANIZATION ICD-10: F43.1


Definition: A disorder characterized by the development either of a single delusion or of a set of related delusions that are usually persistent and sometimes lifelong. The content of the delusion or delusions is very variable. Clear and persistent auditory hallucinations (voices), schizophrenic symptoms such as delusions of control and marked blunting of affect, and definite evidence of brain disease are all incompatible with this diagnosis. However, the presence of occasional or transitory auditory hallucinations, particularly in elderly patients, does not rule out this diagnosis, provided that they are not typically schizophrenic and fo ...[+++]

Définition: Trouble caractérisé par la survenue d'une idée délirante unique ou d'un ensemble d'idées délirantes apparentées, habituellement persistantes, parfois durant toute la vie. Le contenu de l'idée ou des idées délirantes est très variable. La présence d'hallucinations auditives (voix) manifestes et persistantes, de symptômes schizophréniques tels que des idées délirantes d'influence ou un émoussement net des affects, ou la mise en évidence d'une affection cérébrale, sont incompatibles avec le diagnostic. Toutefois, la présence d'hallucinations auditives, en particulier chez les sujets âgés, survenant de façon irrégulière ou transi ...[+++]
WORLD HEALTH ORGANIZATION ICD-10: F22.0
WORLD HEALTH ORGANIZATION ICD-10: F22.0


A rare cancer of corpus uteri presenting as a large, polypoid, intraluminal mass with necrosis, composed of small to intermediate-size, relatively uniform, dyshesive cells displaying no differentiation. It usually presents with dysfunctional bleeding

carcinome indifférencié du corps de l'utérus
SNOMEDCT-BE (disorder) / 766758001
SNOMEDCT-BE (disorder) / 766758001


Definition: The main feature is loss of memory, usually of important recent events, that is not due to organic mental disorder, and is too great to be explained by ordinary forgetfulness or fatigue. The amnesia is usually centred on traumatic events, such as accidents or unexpected bereavements, and is usually partial and selective. Complete and generalized amnesia is rare, and is usually part of a fugue (F44.1). If this is the case, the disorder should be classified as such. The diagnosis should not be made in the presence of organic brain disorders, int ...[+++]

Définition: La caractéristique essentielle est une perte de la mémoire, concernant habituellement des événements importants récents, non due à un trouble mental organique, et trop importante pour être mise sur le compte d'une simple mauvaise mémoire ou d'une fatigue. L'amnésie concerne habituellement des événements traumatisants, tels que des accidents ou des deuils imprévus et elle est le plus souvent partielle et sélective. Une amnésie complète et généralisée est rare, et elle accompagne habituellement une fugue (F44.1); dans ce cas, on doit faire un diagnostic de fugue. On ne doit pas faire ce diagnostic en présence d'un trouble céré ...[+++]
WORLD HEALTH ORGANIZATION ICD-10: F44.0
WORLD HEALTH ORGANIZATION ICD-10: F44.0


A rare hereditary motor and sensory neuropathy characterized by intermediate motor median nerve conduction velocities (usually between 25 and 45 m/s) and signs of both demyelination and axonal degeneration in nerve biopsies. It presents with usual cl

maladie de Charcot-Marie-Tooth intermédiaire autosomique dominante A
SNOMEDCT-BE (usually between 25 and 45 m/s) and signs of both demyelination and axonal degeneration in nerve biopsies. It presents with usual cl / 765744006
SNOMEDCT-BE (disorder) / 765744006


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 self-report data, analysis of blood and other body fluids, characteristic physical and psychological symptom ...[+++]

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 complications, on peut citer: les traumatismes, les fausses routes avec inhalation de vomissements, le delirium, ...[+++]
WORLD HEALTH ORGANIZATION ICD-10: F10-F19
WORLD HEALTH ORGANIZATION ICD-10: F10-F19


A rare hereditary motor and sensory neuropathy characterized by intermediate motor median nerve conduction velocities (usually between 25 and 60 m/s). It presents with moderately severe, slowly progressive usual clinical features of Charcot-Marie-Too

maladie de Charcot-Marie-Tooth intermédiaire autosomique dominante C
SNOMEDCT-BE (usually between 25 and 60 m/s). It presents with moderately severe, slowly progressive usual clinical features of Charcot-Marie-Too / 765746008
SNOMEDCT-BE (disorder) / 765746008


A very rare congenital malformation of the digits with the absence of the middle phalanges (usually of digits two to five), nail dysplasia and duplicated terminal phalanx of the thumb. Has been described in patients from two unrelated families.

brachydactylie type A5
SNOMEDCT-BE (usually of digits two to five), nail dysplasia and duplicated terminal phalanx of the thumb. Has been described in patients from two unrelated families. / 720570007
SNOMEDCT-BE (disorder) / 720570007


A rare endocrine disease with characteristics of the triad of adult-onset diabetes mellitus, progressive hearing loss (usually presenting in the first decade of life and principally of low to moderate frequencies), and/or juvenile-onset optic atrophy

syndrome de Wolfram-like
SNOMEDCT-BE (usually presenting in the first decade of life and principally of low to moderate frequencies), and/or juvenile-onset optic atrophy / 734022008
SNOMEDCT-BE (disorder) / 734022008
IN-CONTEXT TRANSLATIONS


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'usually small'

Date index:2023-08-22 -

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