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Aarskog-like syndrome
Barrett syndrome
Barrett ulcer
Chronic peptic ulcer and esophagitis syndrome
Columnar-like esophagus
Esophagitis-peptic ulcer
Flu-like syndrome
Gastroesophageal reflux
Histamine-like syndrome
Influenza-like syndrome
Myopathy in rheumatoid arthritis
Scleroderma
Scleroderma-like syndrome
Sicca syndrome
Sjögren
Systemic lupus erythematosus

Traduction de «scleroderma-like syndrome » (Anglais → Français) :

scleroderma-like syndrome

syndrome pseudosclérodermique


influenza-like syndrome | flu-like syndrome

syndrome d'allure grippale | SAG


Aarskog-like syndrome

syndrome faciodigitogénital autosomique récessif


A rare Huntington disease-like syndrome with characteristics of childhood-onset progressive neurologic deterioration with pyramidal and extrapyramidal abnormalities, chorea, dystonia, ataxia, gait instability, spasticity, seizures, mutism, and (on br

maladie de Huntington-like 3


Larsen-like syndrome, lethal type, has characteristics of multiple joint dislocation and respiratory insufficiency due to tracheomalacia and or lung hypoplasia. It has been described in less than ten patients. Transmission is thought to be autosomal

syndrome létal de Larsen-like




Barrett syndrome | Barrett ulcer | columnar-like esophagus | chronic peptic ulcer and esophagitis syndrome | esophagitis-peptic ulcer | gastroesophageal reflux

syndrome de Barrett | œsophagite | œsophage de Barrett | épithélium de Barrett


Myopathy in:rheumatoid arthritis (M05-M06+) | scleroderma (M34.8+) | sicca syndrome [Sjögren] (M35.0+) | systemic lupus erythematosus (M32.1+)

Myopathie au cours de:lupus érythémateux disséminé (M32.1+) | arthrite rhumatoïde (M05-M06+) | sclérodermie (M34.8+) | syndrome de Gougerot-Sjögren (M35.0+)


Bronze baby syndrome Neonatal scleroderma Urticaria neonatorum

Sclérodermie néonatale Syndrome du bébé bronzé Urticaire du nouveau-né




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Date index: 2022-01-08
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