Kenza Bouayed
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View article: Secondary congenital nephrotic syndrome complicated by acute mesenteric ischemia: A case report
Secondary congenital nephrotic syndrome complicated by acute mesenteric ischemia: A case report Open
Thromboembolic events are among the most serious, yet rare complications of nephrotic syndrome. While peripheral venous thrombosis and pulmonary embolism are the most common, superior mesenteric artery thrombosis is a rare but life-threate…
View article: Phenotype–genotype correlation in children with familial Mediterranean fever in Morocco
Phenotype–genotype correlation in children with familial Mediterranean fever in Morocco Open
Joint involvement is more common in the M694V genotype, and the genetic profile shows different results compared to neighboring countries.
View article: Disease evolution in systemic juvenile idiopathic arthritis: an international, observational cohort study through JIRcohort
Disease evolution in systemic juvenile idiopathic arthritis: an international, observational cohort study through JIRcohort Open
View article: Access to Care and Therapy for Kawasaki Disease in the Arab Countries: A Kawasaki Disease Arab Initiative (Kawarabi) Multicenter Survey:
Access to Care and Therapy for Kawasaki Disease in the Arab Countries: A Kawasaki Disease Arab Initiative (Kawarabi) Multicenter Survey: Open
Kawasaki Disease (KD) is still the most common acquired heart disease in children below the age of five years; it has been well described in the developed world; however, data from the Arab world are limited to case reports or single-cente…
View article: Efficacy of Anakinra Treatment in two Moroccan Patients With Mevalonate Kinase Deficiency
Efficacy of Anakinra Treatment in two Moroccan Patients With Mevalonate Kinase Deficiency Open
Mevalonate kinase deficiency (MKD) is a rare hereditary autoinflammatory disease, with a widely variable clinical spectrum. It is characterized by febrile recurrent episodes and systemic inflammation. Data on therapeutic options for MKD ar…
View article: 58 Comparison of the 2015 pediatric diagnostic criteria for Behcet’s disease with the 2014 and 1990 International Study Group Diagnostic Criteria
58 Comparison of the 2015 pediatric diagnostic criteria for Behcet’s disease with the 2014 and 1990 International Study Group Diagnostic Criteria Open
Background Behçet's disease is a multisystem vasculitis whose pathogenesis remains unclear. Although usually described in young adults, it may begin in childhood. The diagnosis is clinical, based on international criteria. The limitations …
View article: Biotherapy in juvenile idiopathic arthritis Moroccan patients: a single center experience
Biotherapy in juvenile idiopathic arthritis Moroccan patients: a single center experience Open
In this study, we aimed to evaluate the clinicobiological findings and the biotherapy treatment response of Moroccan patients with juvenile idiopathic arthritis (JIA), and compare our results with those of populations of the same or differ…
View article: Epidemiology and demographics of juvenile idiopathic arthritis in Africa and Middle East
Epidemiology and demographics of juvenile idiopathic arthritis in Africa and Middle East Open
View article: Dilated Cardiomyopathy in Systemic Lupus Erythematosus: A Pediatric Case Report
Dilated Cardiomyopathy in Systemic Lupus Erythematosus: A Pediatric Case Report Open
Background: Systemic lupus erythematosus (SLE) is a chronic inflammatory autoimmune disease that can affect any organ in the body, nonetheless cardiac involvement is frequent. Pericarditis is the most common type of heart attack followed b…
View article: Aortic Regurgitation Complicating Polyarticular Juvenile Idiopathic Arthritis
Aortic Regurgitation Complicating Polyarticular Juvenile Idiopathic Arthritis Open
Juvenile idiopathic arthritis (JIA), defined by the onset of arthritis evolving for more than 6 months, before the age of 16 years old, with no evident etiology. It is the most common type of arthritis in children under the age of 16. The …
View article: Dilated cardiomyopathy: A rare and late complication of the hemolytic-uremic syndrome
Dilated cardiomyopathy: A rare and late complication of the hemolytic-uremic syndrome Open
View article: Bicipital synovial cyst in poly-articular juvenile idiopathic arthritis
Bicipital synovial cyst in poly-articular juvenile idiopathic arthritis Open
Background: Large synovial cysts are rare in juvenile idiopathic arthritis ( JIA).They are usually located in popliteal area.Bicipital cyst is uncommon and has been described in systemic onset of JIA during an inflammatory attack.We descri…
View article: Consensus classification criteria for paediatric Behçet's disease from a prospective observational cohort: PEDBD
Consensus classification criteria for paediatric Behçet's disease from a prospective observational cohort: PEDBD Open