Objectives The aim of this study was to investigate the faecal carriage and molecular
epidemiology of extended-spectrum β-lactamase (ESBL)-producing Enterobacteriaceae (ESBLE) …

Recurrent respiratory tract infections are one of the most frequent reasons for pediatric visits
and hospitalization. Causes of this pathology are multiple ranging from congenital to …

Juvenile dermatomyositis is a rare disorder, but remains the most commonly occurring chronic
inflammatory myopathy among children. Other than the proximal muscles and skin, which …

Severe neonatal hypernatremia is an important electrolyte disorder that has serious effects.
Cerebral venous thrombosis and aortic thrombosis are relatively rare in severe neonatal …

This study was conducted in order to assess the acquisition rate of Acinetobacter baumannii
by newborn screening, on admission and during the discharge process of neonatal …

La maladie de Wilson ou dégénérescence hépato-lenticulaire est une affection génétique
autosomique récessive caractérisée par une accumulation toxique de cuivre dans l'organisme…

Congenital lobar emphysema (CLE) is a rare cause of respiratory distress during the neonate
period. It is characterized by overinflation of pulmonary lobe, most commonly the left upper …

Anti-D isoimmunisation remains the most common cause of erythroblastosis fetalis. Whereas
most clinically significant blood group sensitisations noted during pregnancy are still …

Farber disease is a rare lysosomal storage disease characterized by a clinical triad
including painful joint deformity, subcutaneous nodules and hoarseness, due to progressive …

We report a case of a 10-year-old girl who presented with an acute neurological deficit
preceded by a 2 month history of headaches. The patient was treated for acute viral encephalitis …