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Charcot fever
Charcot intermittent hepatic fever
Charcot triad
Charcot's triad
Clutton's joints+
Color triad
Colour triad
Disease Charcot-Marie-Tooth
Déjerine-Sottas
Encephalitis+
Late congenital cardiovascular syphilis+
Meningitis+
Optic atrophy+
Osteochondropathy+
Polyneuropathy+
Retrobulbar neuritis+
Syphilitic arthropathy+
Syphilitic parkinsonism+
Syphilitic saddle nose
Triad

Vertaling van "charcot triad " (Engels → Nederlands) :





Charcot fever | Charcot intermittent hepatic fever

febris intermittens hepaticus | koorts van Charcot


Charcot-Marie-Tooth disease, type 4B2 (CMT4B2) is a severe early-onset demyelinating CMT peripheral sensorimotor polyneuropathy. Clinically and pathologically very similar to Charcot-Marie-Tooth type 4B1 with childhood-onset of muscle weakness, senso

ziekte van Charcot-Marie-Tooth type 4B2


A rare hereditary motor and sensory neuropathy characterized by intermediate motor median nerve conduction velocities (usually between 25 and 60 m/s). It presents with moderately severe, slowly progressive usual clinical features of Charcot-Marie-Too

autosomaal dominante intermediaire ziekte van Charcot-Marie-Tooth type C


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

syndroom van Graham Little


Clutton's joints+ (M03.1*) Hutchinson's:teeth | triad | Late congenital:cardiovascular syphilis+ (I98.0*) | syphilitic:arthropathy+ (M03.1*) | osteochondropathy+ (M90.2*) | Syphilitic saddle nose

Elke congenitale syfilitische aandoening gespecificeerd als laat of zich manifesterend vanaf tweede jaar na geboorte. | gewrichten van Clutton (M03.1) | Hutchinson- | tanden | Hutchinson- | trias | late congenitale | cardiovasculaire-syfilis (I98.0) | late congenitale | syfilitische- | artropathie (M03.1) | late congenitale | syfilitische- | osteochondropathie (M90.2) | syfilitische zadelneus


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

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


Charcot's arthropathy+ (M14.6*) Late syphilitic:acoustic neuritis+ (H94.0*) | encephalitis+ (G05.0*) | meningitis+ (G01*) | optic atrophy+ (H48.0*) | polyneuropathy+ (G63.0*) | retrobulbar neuritis+ (H48.1*) | Syphilitic parkinsonism+ (G22*) Tabes dorsalis

artropathie van Charcot (M14.6) | late syfilitische(-) | encefalitis (G05.0) | late syfilitische(-) | meningitis (G01) | late syfilitische(-) | retrobulbaire-neuritis (H48.1) | late syfilitische{-) | neuritis acustica (H94.0) | late syfilitische(-) | opticusatrofie (H48.0) | late syfilitische(-) | polyneuropathie (G63.0) | syfilitisch parkinsonisme (G22) | tabes dorsalis




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Date index: 2024-02-26
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