Introduction: Pediatric Multisystem Inflammatory Syndrome linked to temporal with SARS-Cov2 is a new hyper inflammatory disorder that affects children with Covid-19 infection. It usually occurs 2 to 6 weeks following illness or exposure. Materials and Methods: Descriptive retrosp...
Open access
Research Article10.9734/ajpr/2022/v10i4203
We present different cases of cardiovascular abnormalities in 3 patients with WS aged between 8months and 7 years. Williams-Beuren Syndrome is characterized by specific facial dysmorphism that may look like an “elfin face”, congenital heart diseases, cognitive disorder, social pe...
Open access
Research Article10.9734/ajpr/2022/v9i330268
Aortopulmonary window (APW) is an uncommon congenital cardiac malformation, accounting for 0.1% of all congenital cardiac diseases. It is a defect between the ascending aorta and the trunk of the pulmonary artery. Such abnormality may occur as an isolated lesion or it can be asso...
Open access
Research Article10.9734/ajpr/2021/v7i130206
Aims: To describe mortality and morbidity among preterm infants who died during hospitalization in a Moroccan tertiary center and to contextualize findings with the literature. Study Design: Retrospective case analysis and literature review. Setting and Period: NICU, HMIMV, Rabat...
Open access
Research Article10.9734/ajarr/2025/v19i101189
Background: Hydranencephaly is a rare congenital brain malformation with an incidence estimated to be between 1 in 10 000 and 1 in 5 000 pregnancies. It is characterized by the absence of development of the cerebral hemispheres, which are replaced by cerebrospinal fluid. The diag...
Open access
Research Article10.9734/ajpr/2024/v14i8377
Introduction: Congenital nasal pyriform aperture stenosis is a rare cause of neonatal respiratory distress. Observation: A female neonate was born by cesarean section at 39 SA for hydramnios, triple scarred uterus and macrosomia. He was macrosomic and had no facial dysmorphia, he...
Open access
Research Article10.9734/ajpr/2023/v13i3278
Triple X syndrome is a relatively common chromosomal abnormality affecting 0.1% of live-born girls. Most of these girls have a normal phenotype and only a few cases have birth defects. The diagnosis of triple X syndrome may never be made because the clinical manifestations are no...
Open access
Research Article10.9734/ajpr/2023/v11i2214
Hydrops fetalis is defined by the accumulation of fluids in the serous membranes (pleurisy, ascites, pericarditis...), it is a rare condition; its etiologies are divided into immunological and non-immunological. Supraventricular tachycardia remains a known cause, non-immunologica...
Open access
Research Article10.9734/ajpr/2022/v10i2194