Noonan syndrome is a common autosomal dominant disorder characterized by short stature,
congenital heart disease and facial dysmorphia with an incidence of 1/1000 to 2500 live …

Drug-induced hypersensitivity or Drug Reaction with Eosinophilia and Systemic Symptom (DRESS)
is a severe adverse drug-induced reaction. Diagnosing DRESS is challenging due …

Purpose Rare genetic variants in KDR, encoding the vascular endothelial growth factor
receptor 2 (VEGFR2), have been reported in patients with tetralogy of Fallot (TOF). However, …

Background In the Neonatal Intensive Care Unit, preterm neonates present a neurodevelopmental
risk expressed by physiological and behavioral signs that are difficult to interpret. This …

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 …

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

The objective of our work is to study the multi-systemic inflammatory syndrome (PIMS) in
children, to determine its frequency, by analyzing the epidemiological, clinical, paraclinical, …

The aim of this article is to give a definition of K-frames in Krein spaces. This definition is
compatible with K-frames already known in Hilbert spaces and it generalizes them. We will …

Multicentric Castleman’s disease is a rare benign and unexplained lymphoproliferative
disorder that is extremely uncommon in children. It presents with fever, systemic symptoms, …

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 …