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Aarskog
Angina cruris
Angiosclerotica intermittens
Carotis-sinus syndroom
Charcot-Marie-Tooth
Claudicatio angiosclerotica intermittens
Claudicatio intermittens
Cockayne
De Lange
Dubowitz
Dysbasia
Déjerine-Sottas
Holt-Oram
Infantiele hypertrofische-neuropathie
Intermitterend hinken
Klippel-Trenaunay-Weber
LBWC
Nagel-patella
Noonan
Prader-Willi
Robinow-Silverman-Smith
Rubinstein-Taybi
Russell-Silver
Seckel
Sirenomelie
Smith-Lemli-Opitz
Syndroom
Syndroom
Syndroom van
Syndroom van Charcot
Syndroom van Charcot-Weiss-Baker
Syndroom van Roussy-Lévy
TAR-syndroom
Trombocytopenie met ontbreken van radius
VATER-syndroom
Ziekte van
Ziektebeeld

Traduction de «Syndroom van Charcot » (Néerlandais → Anglais) :

carotis-sinus syndroom | syndroom van Charcot-Weiss-Baker

Charcot-Weiss-Baker syndrome


angina cruris | claudicatio angiosclerotica intermittens | claudicatio intermittens | dysbasia | intermitterend hinken | syndroom van Charcot

intermittent claudication


angina cruris | angiosclerotica intermittens | claudicatio intermittens | dysbasia | syndroom van Charcot

angina cruris | crural angina


hereditaire motorische- en sensorische-neuropathie, type I-IV | infantiele hypertrofische-neuropathie | peroneale spieratrofie (axonaal type)(hypertrofisch type) | syndroom van Roussy-Lévy | ziekte van | Charcot-Marie-Tooth | ziekte van | Déjerine-Sottas

Disease:Charcot-Marie-Tooth | Déjerine-Sottas | Hereditary motor and sensory neuropathy, types I-IV Hypertrophic neuropathy of infancy Peroneal muscular atrophy (axonal type)(hypertrophic type) Roussy-Lévy syndrome




syndroom van | Aarskog | syndroom van | Cockayne | syndroom van | de Lange | syndroom van | Dubowitz | syndroom van | Noonan | syndroom van | Prader-Willi | syndroom van | Robinow-Silverman-Smith | syndroom van | Russell-Silver | syndroom van | Seckel | syndroom van | Smith-Lemli-Opitz

Syndrome:Aarskog | Cockayne | De Lange | Dubowitz | Noonan | Prader-Willi | Robinow-Silverman-Smith | Russell-Silver | Seckel | Smith-Lemli-Opitz


syndroom (van) | Holt-Oram | syndroom (van) | Klippel-Trenaunay-Weber | syndroom (van) | nagel-patella | syndroom (van) | Rubinstein-Taybi | syndroom (van) | sirenomelie | TAR-syndroom [trombocytopenie met ontbreken van radius] | VATER-syndroom

Syndrome:Holt-Oram | Klippel-Trénaunay-Weber | nail patella | Rubinstein-Taybi | sirenomelia | thrombocytopenia with absent radius [TAR] | VATER


LBWC (limb body wall complex)-syndroom

Limb body wall complex


SOLAMEN (segmental outgrowth, lipomatosis, arteriovenous malformation, epidermal nevus)-syndroom

A rare genetic, poly malformative syndrome with characteristics of progressive, proportionate, asymmetric segmental overgrowth (with soft tissue hypertrophy and ballooning effect) that develops and progresses rapidly in early childhood, arteriovenous


AHO-PHP (Albright hereditary osteodystrophy, pseudohypoparathyroidism)-syndroom Ia

Pseudohypoparathyroidism type Ia




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Date index: 2024-04-28
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