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Translation of "short legs small " (English → French) :

This syndrome has characteristics of severe short stature with disproportionately short legs, small hands, clinodactyly, valvular heart disease and dysmorphism (ptosis, high-arched palate, abnormal dentition). It has been described in a mother and tw

syndrome de petite taille-valvulopathie cardiaque-dysmorphie
SNOMEDCT-BE (ptosis, high-arched palate, abnormal dentition). It has been described in a mother and tw / 716193004
SNOMEDCT-BE (disorder) / 716193004


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 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


A very rare syndrome described in three siblings of one Japanese family with main features of congenital heart disease, round face with depressed nasal bridge, small mouth, short stature, and relatively dark skin and typical dermatoglyphic anomalies,

syndrome de cardiopathie congénitale-face ronde-petite taille
SNOMEDCT-BE (disorder) / 715987000
SNOMEDCT-BE (disorder) / 715987000


A condition with multiple abnormalities including mild to severe intellectual disability, impaired growth from birth leading to short stature, and microcephaly. Affected individuals may also have distinctive facial features (including a small forehea

syndrome de cassure chromosomique de Varsovie
SNOMEDCT-BE / 702829000
SNOMEDCT-BE (disorder) / 702829000


This syndrome has characteristics of intellectual deficit, muscle wasting, short stature, a prominent lower lip, small testes, kyphosis and joint hyperextensibility. An abnormal gait, tremor, decreased fine motor coordination and impaired speech are

syndrome de Cabezas
SNOMEDCT-BE (disorder) / 719811001
SNOMEDCT-BE (disorder) / 719811001


This syndrome has characteristics of short stature, anterior pituitary hormone deficiency, small sella turcica and a hypoplastic anterior hypophysis associated with pointed cerebellar tonsils. It has been described in three generations of large Frenc

syndrome de petite taille-anomalies hypophysaires et cérébelleuses-selle turcique anormale
SNOMEDCT-BE (disorder) / 721072003
SNOMEDCT-BE (disorder) / 721072003


A rare benign non-Langerhans cell histiocytosis characterized by childhood or adolescence onset of multiple, small, asymptomatic, slowly progressing, skin-colored to red-brown papules with predilection for the face, dorsal hands, forearms and legs, w

histiocytose progressive mucineuse héréditaire
SNOMEDCT-BE (disorder) / 771300001
SNOMEDCT-BE (disorder) / 771300001




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'short legs small'

Date index:2022-02-15 -

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