Vertaling van "aarskog-like syndrome " (Engels → Frans) :

Aarskog-like syndrome
syndrome faciodigitogénital autosomique récessif

influenza-like syndrome | flu-like syndrome
syndrome d'allure grippale | SAG

scleroderma-like syndrome
syndrome pseudosclérodermique

Histamine-like syndrome
Syndrome de type histaminique

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

Syndrome:Aarskog | Cockayne | De Lange | Dubowitz | Noonan | Prader-Willi | Robinow-Silverman-Smith | Russell-Silver | Seckel | Smith-Lemli-Opitz
Syndrome de:Aarskog | Cockayne | De Lange | Dubowitz | Noonan | Prader-Willi | Robinow-Silverman-Smith | Russell-Silver | Seckel | Smith-Lemli-Opitz

Beta-glucuronidase deficiency Mucopolysaccharidosis, types III, IV, VI, VII Syndrome:Maroteaux-Lamy (mild)(severe) | Morquio(-like)(classic) | Sanfilippo (type B)(type C)(type D)
Carence en bêta-glucoronidase Mucopolysaccharidoses, type III, IV, VI, VII Syndrome de:Maroteaux-Lamy (léger) (sévère) | Morquio (-semblable à) (classique) | Sanfilippo (type B) (type C) (type D)