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External limb prosthesis
Inferior extremity
Inferior limb
Inferior member
Leg
Leg prosthesis
Lower bow limb
Lower extremity
Lower extremity prosthesis
Lower extremity prosthetic device
Lower leg
Lower limb
Lower-limb phlebography
Lower-limb prosthesis
Lower-limb venography
Pelvic limb
Shank

Translation of "Lower-limb prosthesis " (English → French) :

lower extremity prosthesis [ lower extremity prosthetic device | lower-limb prosthesis | leg prosthesis ]

prothèse du membre inférieur [ prothèse de jambe | prothèse jambière ]
Prostheses
Prothèses


lower limb [ lower extremity | inferior limb | inferior member | pelvic limb | leg | shank | inferior extremity ]

membre inférieur [ membre abdominal | membre pelvien | jambe ]
Water Transport
Appareil locomoteur (Médecine)


lower-limb phlebography | lower-limb venography

phlébographie des membres inférieurs
IATE - Health
IATE - Health


lower bow limb [ lower limb ]

branche inférieure de l'arc [ branche inférieure ]
Archery
Tir à l'arc


lower limb | lower extremity | inferior limb | leg

membre inférieur | membre pelvien | membre abdominal | jambe
médecine > anatomie
médecine > anatomie


lower leg | lower limb

branche aval
IATE - Mechanical engineering | Building and public works
IATE - Mechanical engineering | Building and public works


external limb prosthesis

prothèse de membre externe
IATE - Health
IATE - Health


Disease with characteristics of muscle weakness and atrophy in the lower limbs, most severely affecting the quadriceps. The loss of motor neurons leads to atrophy of the muscles in the lower limbs with manifestations including unsteady walk and walki

amyotrophie spinale proximale autosomique dominante de l'enfance
SNOMEDCT-BE (disorder) / 772129007
SNOMEDCT-BE (disorder) / 772129007


A rare subtype of autosomal recessive intermediate Charcot-Marie-Tooth (CMT) disease with characteristics of childhood to adulthood-onset of progressive, moderate to severe, predominantly distal, mostly lower limb muscle weakness and atrophy, foot de

maladie de Charcot-Marie-Tooth intermédiaire autosomique récessive type C
SNOMEDCT-BE (CMT) disease with characteristics of childhood to adulthood-onset of progressive, moderate to severe, predominantly distal, mostly lower limb muscle weakness and atrophy, foot de / 773414009
SNOMEDCT-BE (disorder) / 773414009


A rare hereditary motor and sensory neuropathy disorder with characteristics of the typical CMT phenotype (slowly progressive distal muscle atrophy and weakness in upper and lower limbs, distal sensory loss in extremities, reduced or absent deep tend

maladie de Charcot-Marie-Tooth intermédiaire autosomique dominante type F
SNOMEDCT-BE (slowly progressive distal muscle atrophy and weakness in upper and lower limbs, distal sensory loss in extremities, reduced or absent deep tend / 770759001
SNOMEDCT-BE (disorder) / 770759001




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'Lower-limb prosthesis'

Date index:2023-07-03 -

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