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Dysostose de type Pfaundler-Hurler
Dysostose multiple
Dysostosis multiplex
Dystrophie de Hurler-Ellis
Gargoylisme
Gargoïlisme
Lipochondrodystrophie
Lipocondrodystrophie
MPS I
MPS I-H
Maladie de Hunter-Hurler
Maladie de Hurler
Maladie de Pfaundler-Hurler
Maladie à inclusion cellulaire
Muccopolysaccharidose
Mucolipidose II
Mucolipidose III
Mucopolysaccharidose 1
Mucopolysaccharidose de type 1
Mucopolysaccharidose de type I
Nanisme à type de gargouille
Polydystrophie de Hurler
Polydystrophie de type Hurler
Syndrome d'Ellis-Sheldon
Syndrome de Hurler
Syndrome de Pfaundler-Hurler

Translation of "maladie de pfaundler-hurler " (French → English) :

TERMINOLOGY
see also In-Context Translations below
gargoylisme | gargoïlisme | dysostosis multiplex | dysostose de type Pfaundler-Hurler | dystrophie de Hurler-Ellis | lipocondrodystrophie | maladie de Hunter-Hurler | maladie de Hurler | maladie de Pfaundler-Hurler | muccopolysaccharidose | nanisme à type de gargouille | syndrome d'Ellis-Sheldon | polydystrophie de Hurler

gargoylism | Hunter's syndrome | Hunter-Hurler syndrome | Hurler's disease | Hurler's polydystrophy | Hurler's syndrome | Johnie McL.'s syndrome | Pfaundler-Hurler syndrome | Sheldon-Ellis syndrome | Thompson's syndrome | dysostosis multiplex | dysostotic idiocy | lipochondrodystrophy | mucopolysaccharidosis
biologie > embryologie | biologie > génétique | médecine > sémiologie et pathologie
biologie > embryologie | biologie > génétique | médecine > sémiologie et pathologie


dysostose multiple | gargoylisme | lipochondrodystrophie | maladie de Hurler | mucopolysaccharidose de type I | syndrome de Hurler | syndrome de Pfaundler-Hurler | MPS I [Abbr.] | MPS I-H [Abbr.]

dysostosis multiplex | gargoylism | Hurler syndrome | Hurler's disease | Hurler's syndrome | lipochondrodystrophy | mucopolysaccharidosis I | mucopolysaccharidosis type I-H | Pfaundler-Hurler syndrome | MPS I [Abbr.] | MPS I-H [Abbr.]
IATE - Health
IATE - Health


Mucolipidose II [maladie à inclusion cellulaire] Mucolipidose III [polydystrophie de type Hurler]

Mucolipidosis II [I-cell disease] Mucolipidosis III [pseudo-Hurler polydystrophy]
WORLD HEALTH ORGANIZATION ICD-10: E77.0
WORLD HEALTH ORGANIZATION ICD-10: E77.0


mucopolysaccharidose de type 1 [ mucopolysaccharidose 1 | maladie de Hurler ]

mucopolysaccharidosis IH [ Hurler's syndrome | Hurler-Pfaundler syndrome ]
Os et articulations
Bones and Joints
IN-CONTEXT TRANSLATIONS
On parle d'un montant d'environ 250 000 $ annuellement pour les enzymes de remplacement dans le traitement de la maladie de Fabry ou encore de près de 400 000 $ par année pour traiter le syndrome de Hurler.

I am talking about $250,000 a year for replacement enzymes to treat Fabry disease or close to $400,000 a year to treat Hurler's syndrome.


Ces patients combattent chaque jour la maladie de Pompe, de Fabry, de Hurler, ou de Gaucher, pour ne nommer que celles-ci.

Every day, these patients are fighting Pompe's disease, Fabry disease, Hurler's syndrome, or Gaucher disease, to name a few.




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maladie de pfaundler-hurler

Date index:2024-05-01 -

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