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Aran-Duchenne disease
Cruveilhier disease
DMD
Duchenne disease
Duchenne dystrophy
Duchenne muscular dystrophy
Duchenne type muscular dystrophy
Duchenne's muscular dystrophy
Duchenne-Griesinger disease
Enzootic muscular dystrophy
Erb atrophy
Erb dystrophy
Facioscapulohumeral muscular atrophy
Facioscapulohumeral muscular dystrophy
Infantile spinal muscular atrophy
Kennedy disease
Kennedy's disease
Landouzy-Dejerine dystrophy
Meryon's disease
Muscular dystrophy
Muscular dystrophy - Duchenne type
Muscular steatosis
Nutritional muscular dystrophy
PMA
Progressive muscular atrophy
Progressive muscular atrophy of infancy
Progressive spinal muscular atrophy
Pseudohypertrophic muscular dystrophy
SBMA
SMA
SMA I
SPMA
Severe infantile spinal muscular atrophy
Spinal and bulbar muscular atrophy
Spinal muscular atrophy
Spinal muscular atrophy type I
Spinal progressive muscular atrophy
Spinobulbar muscular atrophy
Werdnig-Hoffman disease
White muscle disease
X-linked spinal and bulbar muscular atrophy
Zimmerlin atrophy

Traduction de «muscular steatosis » (Anglais → Français) :



Duchenne muscular dystrophy | Duchenne type muscular dystrophy | Duchenne's muscular dystrophy | Meryon's disease | Muscular dystrophy - Duchenne type | pseudohypertrophic muscular dystrophy | DMD [Abbr.]

dystrophie musculaire de Duchenne | myopathie de Duchenne | myopathie primitive progressive pseudo-hypertrophique type Duchenne-Griesinger | myopathie pseudo-hypertrophique de Duchenne | DMD [Abbr.]


Aran-Duchenne disease | Cruveilhier disease | PMA | progressive muscular atrophy | progressive spinal muscular atrophy | spinal muscular atrophy | spinal progressive muscular atrophy | SMA [Abbr.] | SPMA [Abbr.]

amyotrophie d'Aran-Duchenne | amyotrophie spinale progressive | atrophie de Cruveilhier | atrophie musculaire progressive d'Aran | maladie d'Aran-Duchenne


infantile spinal muscular atrophy | progressive muscular atrophy of infancy | severe infantile spinal muscular atrophy | spinal muscular atrophy type I | Werdnig-Hoffman disease | SMA I [Abbr.]

amyotrophie spinale infantile sévère | amyotrophie spinale progressive de type I | atrophie spinale progressive infantile | maladie de Werdnig-Hoffmann | syndrome de Werdnig-Hoffmann


muscular dystrophy [ nutritional muscular dystrophy | enzootic muscular dystrophy | white muscle disease ]

maladie du muscle blanc [ maladie des muscles blancs | dystrophie musculaire nutritionnelle | dystrophie musculaire ]


spinal and bulbar muscular atrophy | SBMA | Kennedy disease | X-linked spinal and bulbar muscular atrophy | spinobulbar muscular atrophy | Kennedy's disease

maladie de Kennedy | atrophie musculaire spinale et bulbaire | atrophie spinale bulbo-musculaire | amyotrophie spinobulbaire | SBMA


Landouzy-Dejerine dystrophy [ facioscapulohumeral muscular dystrophy | facioscapulohumeral muscular atrophy ]

myopathie facio-scapulo-humérale de Landouzy Déjerine [ myopathie facio-scapulo-humérale | myopathie de Landouzy-Déjerine ]


Duchenne muscular dystrophy [ Duchenne type muscular dystrophy | Duchenne dystrophy | Duchenne disease | Erb dystrophy | Duchenne-Griesinger disease | Zimmerlin atrophy | Erb atrophy ]

maladie de Duchenne de Boulogne


A rare genetic hepatic disease characterized by massive hepatomegaly, moderate to severe transient hypertriglyceridemia and hepatic steatosis (followed by fibrosis) manifesting in infancy with failure to thrive, vomiting, an enlarged abdomen and a fa

hypertriglycéridémie transitoire et stéatose hépatique du nourrisson


An extremely rare genetic endocrine disease with characteristics of primary adrenal insufficiency, dystrophic myopathy, hepatic steatosis, severe psychomotor delay, megalocornea, failure to thrive, chronic constipation, and terminal bladder ectasia w

adrénomyodystrophie


w