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
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
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
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
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