A.laaraj

Familial Hypomagnesemia with Secondary Hypocalcemia: A Challenging Medical Affair

S. Aithmadouch, A.laaraj, A. Radi & R. Abikassem · Asian Journal of Advanced Research and Reports · 2024

Familial or genetic hypomagnesemia with secondary hypocalcemia is a disease typically presenting with epilepsy and characterized by low blood levels of magnesium and calcium and metabolic bone disease, and is caused by mutations in the TRPM6 genes. Various factors such as low die...

Open access Research Article 10.9734/ajarr/2024/v18i12838

A Case Report on Arnold Chiari Type III: Constellation of Disorders, from Diagnosis to Treatment

S.Aithmadouch, k.larbiouassou, A.laaraj & R.abikassem · Asian Journal of Advanced Research and Reports · 2024

Arnold-Chiari type III is a malformation characterised by protrusion of the brainstem, cerebellum and lower part of the brain due to a cranial malformation. It is a rare congenital malformation in which the brain protrudes through a fissure in the skull. It occurs during pregnanc...

Open access Research Article 10.9734/ajarr/2024/v18i12826