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Small bowel

Translation of "only a small " (English → French) :

TERMINOLOGY
see also In-Context Translations below
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


Primary pigmented nodular adrenocortical disease (PPNAD) is a form of bilateral adrenocortical hyperplasia that is often associated with adrenocorticotrophin hormone independent Cushing syndrome. The disease has characteristics of small to normal siz

dysplasie micronodulaire pigmentée des surrénales
SNOMEDCT-BE (PPNAD) is a form of bilateral adrenocortical hyperplasia that is often associated with adrenocorticotrophin hormone independent Cushing syndrome. The disease has characteristics of small to normal siz / 719274008
SNOMEDCT-BE (disorder) / 719274008


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


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


A variant of self-healing collodion baby with manifestation of the presence at birth of a collodion membrane only at the extremities. Only 2 cases were described in the literature. In both cases, the babies healed soon after birth. In one case, molec

bébé collodion à guérison spontanée, forme acrale
SNOMEDCT-BE (disorder) / 718633009
SNOMEDCT-BE (disorder) / 718633009


An extremely rare inborn error of sterol biosynthesis with manifestations of facial dysmorphism, congenital anomalies (including limb and kidney anomalies), failure to thrive, developmental delay and liver disease. Only 4 cases have been reported in

lathostérolose
SNOMEDCT-BE (including limb and kidney anomalies), failure to thrive, developmental delay and liver disease. Only 4 cases have been reported in / 719257008
SNOMEDCT-BE (disorder) / 719257008


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


A rare form of porokeratosis occurring mainly in adolescence and characterised by small pruritic or painful keratotic papules that first appear on the palms and soles, and may gradually become generalised. The prevalence is unknown but it is one of t

porokératose palmoplantaire et disséminée
SNOMEDCT-BE (disorder) / 718218005
SNOMEDCT-BE (disorder) / 718218005


A rare intestinal disorder of neonates of unknown aetiology. Patients are born with a short small bowel (less than 75 cm in length) that compromises proper intestinal absorption and leads chronic diarrhoea, vomiting and failure to thrive.

syndrome du grêle court congénital
SNOMEDCT-BE (less than 75 cm in length) that compromises proper intestinal absorption and leads chronic diarrhoea, vomiting and failure to thrive. / 715201005
SNOMEDCT-BE (disorder) / 715201005


SNOMEDCT-BE (body structure) / 30315005
SNOMEDCT-BE (body structure) / 30315005
IN-CONTEXT TRANSLATIONS


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'only a small'

Date index:2022-07-28 -

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