Boost Your Productivity !Translate documents (Ms-Word, Ms-Excel, ...) faster and better thanks to artificial intelligence!
https://pro.wordscope.com
https://blog. wordscope .com
Diplégie spastique infantile
Féminisation testiculaire
Hyperandrogénisme surrénalien
Hypercorticisme androgénique
Maladie de Little
Maladie de Morris
Maladie de von Willebrand-Jurgens
Myasthénie
Myasthénie grave
Myasthénie grave pseudo-paralytique
Paralysie bulbo-spinale
Pseudo-hermaphrodisme d'Apert et Gallais
Pseudo-hermaphrodisme masculin
Pseudo-hermaphrodisme surrénal
Pseudo-hémophilie A
Pseudo-hémophilie héréditaire
Pseudo-syndrome de Klinefelter
Pseudo-syndrome de Little
Syndrome adréno-génital
Syndrome adrénogénital
Syndrome d'Apert et Gallais
Syndrome d'Apert-Gallais
Syndrome d'Erb
Syndrome d'Erb-Goldflam
Syndrome d'Erb-Oppenheim-Goldflam
Syndrome de Cooke-Apert-Gallais
Syndrome de Gallais
Syndrome de Goldberg-Maxwell-Morris
Syndrome de Graham Little
Syndrome de Graham Little-Piccardi-Lassueur
Syndrome de Hoppe-Goldflam
Syndrome de Little
Syndrome de Minot-von Willebrand
Syndrome de Morris
Syndrome du testicule féminisant
Syndrome génito-surrénal
Syndrome génito-surrénalien
Syndrome génitosurrénal
Syndrome surrénalo-génital
Syndrome surrénalogénital
Syndrome surréno-génital
Syndrome surrénogénital

Translation of "pseudo-syndrome de little " (French → English) :

pseudo-syndrome de Little

pseudo-Little disease syndrome
IATE - Health
IATE - Health


diplégie spastique infantile | maladie de Little | syndrome de Little

Little's disease | spastic diplegia
IATE - Health
IATE - Health


pseudo-syndrome de Klinefelter

pseudo Klinefelter syndrome
IATE - Health
IATE - Health


paralysie périodique avec pseudo-syndrome des loges transitoire

A rare genetic neuromuscular disease characterised by normokalaemic episodes of painful muscle cramping followed by progressive permanent flaccid weakness. Triggered by stress, cold and exercise and associated with myopathic myopathy and painful acut
SNOMEDCT-BE (disorder) / 774153002
SNOMEDCT-BE (disorder) / 774153002


syndrome génitosurrénal | syndrome génito-surrénal | syndrome surrénalogénital | syndrome surrénalo-génital | syndrome surrénogénital | syndrome surréno-génital | syndrome adrénogénital | syndrome adréno-génital | syndrome d'Apert et Gallais | syndrome d'Apert-Gallais | syndrome de Cooke-Apert-Gallais | syndrome de Gallais | hypercorticisme androgénique | hyperandrogénisme surrénalien | syndrome génito-surrénalien | pseudo-hermaphrodisme surrénal | pseudo-hermaphrodisme d'Apert et Gallais

adrenogenital syndrome | suprarenal genital syndrome | Apert-Gallais syndrome | Cooke-Apert-Gallais syndrome | Apert's hirsutism
médecine > endocrinologie | médecine > sémiologie et pathologie
médecine > endocrinologie | médecine > sémiologie et pathologie


myasthénie [ myasthénie grave | syndrome d'Erb-Goldflam | paralysie bulbo-spinale | myasthénie grave pseudo-paralytique | syndrome de Hoppe-Goldflam | syndrome d'Erb | syndrome d'Erb-Oppenheim-Goldflam ]

myasthenia gravis [ MG | Erb disease | progressive bulbar paralysis | Erb-Goldflam syndrome | myasthenia pseudoparalytica | Erb-Oppenheim-Goldflam syndrome | Erb-Goldflam disease | bulbospinal paralysis | Goldflam's disease | Hoppe-Goldflam syndrome | Wilks symptom complex | Wilks syndrome | Goldflam- ]
Système nerveux
Nervous System


féminisation testiculaire | maladie de Morris | pseudo-hermaphrodisme masculin | syndrome de Goldberg-Maxwell-Morris | syndrome de Morris | syndrome du testicule féminisant

testicular feminization | Goldberg-Maxwell syndrome | Goldberg-Maxwell-Morris syndrome | Goldberg-Morris syndrome | Morris syndrome | hairless women syndrome | male pseudohermaphroditism syndrome | testicular feminization syndrome
biologie > génétique | médecine > sémiologie et pathologie
biologie > génétique | médecine > sémiologie et pathologie


maladie de von Willebrand-Jurgens | pseudo-hémophilie A | pseudo-hémophilie héréditaire | syndrome de Minot-von Willebrand

Minot-von Willebrand syndrome | angiohemophilia | von Willebrand's disease | pseudohemophilia | Willebrand's syndrome
médecine
médecine


syndrome de Graham Little-Piccardi-Lassueur

A variant of lichen planopilaris characterised by the clinical triad of progressive cicatricial (scarring) alopecia of the scalp, follicular keratotic papules on glabrous skin, and variable alopecia of the axillae and groin. It is a very rare disease
SNOMEDCT-BE (disorder) / 718215008
SNOMEDCT-BE (scarring) alopecia of the scalp, follicular keratotic papules on glabrous skin, and variable alopecia of the axillae and groin. It is a very rare disease / 718215008


syndrome de Graham Little

A variant of lichen planopilaris characterized by the clinical triad of progressive cicatricial (scarring) alopecia of the scalp, follicular keratotic papules on glabrous skin, and variable alopecia of the axillae and groin. It is a very rare disease
SNOMEDCT-BE (disorder) / 718215008
SNOMEDCT-BE (scarring) alopecia of the scalp, follicular keratotic papules on glabrous skin, and variable alopecia of the axillae and groin. It is a very rare disease / 718215008




www.wordscope.com (v4.0.br.77)

pseudo-syndrome de little

Date index:2022-01-12 -

Pour agences de traduction et traducteurs - For translation agencies & translators

Paris - Brussels - Montreal - Genève - Luxembourg - Madrid

Wordscope - Professional computer-assisted translation tools (CAT tools)