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Maternal care for known or suspected light-for-dates
Placental insufficiency
Small-for-dates
Small-for-dates Small-and-light-for-dates

Translation of "Small-for-dates " (English → French) :

TERMINOLOGY
see also In-Context Translations below
Small-for-dates Small-and-light-for-dates

Petit et léger pour l'âge gestationnel Petit pour l'âge gestationnel
WORLD HEALTH ORGANIZATION ICD-10: P05.1
WORLD HEALTH ORGANIZATION ICD-10: P05.1


Maternal care for known or suspected:light-for-dates | placental insufficiency | small-for-dates

Soins maternels pour cause connue ou présumée de:fœtus léger pour l'âge gestationnel | fœtus petit pour l'âge gestationnel | insuffisance du placenta
WORLD HEALTH ORGANIZATION ICD-10: O36.5
WORLD HEALTH ORGANIZATION ICD-10: O36.5


A rare syndrome consisting of growth retardation, facial dysmorphism, camptodactyly and skeletal anomalies. To date only eight cases have been reported in the literature. Dysmorphic features include flat face, epicanthic folds, telecanthus, small dow

camptodactylie de Guadalajara type 1
SNOMEDCT-BE (disorder) / 720602007
SNOMEDCT-BE (disorder) / 720602007


A rare X-linked inherited type of ocular albinism described in one African kindred (7 males over 3 generations) to date with characteristics of severe visual impairment, translucent pale-blue irides, a reduction in the retinal pigment and moderately

albinisme oculaire avec surdité sensorielle tardive
SNOMEDCT-BE (7 males over 3 generations) to date with characteristics of severe visual impairment, translucent pale-blue irides, a reduction in the retinal pigment and moderately / 722054007
SNOMEDCT-BE (disorder) / 722054007


Disease with characteristics of early-onset cerebellar signs, eye movement abnormalities and pyramidal signs. Fifty-one clinically affected members from four families (of British, Pakistani, German and French descent) have been reported to date. The

ataxie spinocérébelleuse type 11
SNOMEDCT-BE (of British, Pakistani, German and French descent) have been reported to date. The / 719207000
SNOMEDCT-BE (disorder) / 719207000


A very rare subtype of autosomal dominant cerebellar ataxia type 3 with characteristics of late-onset and slowly progressive cerebellar signs (gait ataxia) and eye movement abnormalities. To date, only 23 affected patients have been described from on

ataxie spinocérébelleuse type 26
SNOMEDCT-BE (gait ataxia) and eye movement abnormalities. To date, only 23 affected patients have been described from on / 718769009
SNOMEDCT-BE (disorder) / 718769009


An extremely rare tumour association characterised by dual predisposition to melanoma and neural system tumours (typically astrocytoma). Fewer than 20 affected families have been reported to date. Affected individuals had cutaneous melanoma in associ

syndrome mélanome-tumeur du système nerveux
SNOMEDCT-BE (typically astrocytoma). Fewer than 20 affected families have been reported to date. Affected individuals had cutaneous melanoma in associ / 717968005
SNOMEDCT-BE (disorder) / 717968005


Cap polyposis (CP) is characterised by multiple inflammatory polyps that predominantly affect the rectosigmoid area and manifest primarily as rectal bleeding with abnormal transit, constipation or diarrhoea. To date, around 67 cases have been describ

cap polypose
SNOMEDCT-BE (CP) is characterised by multiple inflammatory polyps that predominantly affect the rectosigmoid area and manifest primarily as rectal bleeding with abnormal transit, constipation or diarrhoea. To date, around 67 cases have been describ / 7206
SNOMEDCT-BE (disorder) / 720604008


This syndrome has characteristics of X-linked intellectual deficit and mild variable manifestations, including short stature, small head circumference, sloping forehead, hearing loss, abnormally shaped ears, and small testes. It has been described in

déficience intellectuelle liée à l'X type Abidi
SNOMEDCT-BE (disorder) / 719018008
SNOMEDCT-BE (disorder) / 719018008


An extremely rare subtype of renal cell carcinoma most frequently characterized by a small, solitary, well-circumscribed, unencapsulated renal tumor composed of multiple small to medium-sized cysts with a white or gray, spongy (bubble wrap-like ) cut

carcinome rénal tubulokystique
SNOMEDCT-BE (bubble wrap-like") cut / 733603009
SNOMEDCT-BE (disorder) / 733603009
IN-CONTEXT TRANSLATIONS


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'Small-for-dates'

Date index:2021-04-12 -

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