Objective: Invasive aspergillosis of the central nervous system in immunocompetent patients
is a rare disease. We present in this study three cases that were treated in our centre and …

Objective To evaluate the ability of preoperative mastoid high resolution Computerized
tomography (CT Scan) fusion with the postoperative diffusion weighted magnetic resonance …

Objective EAST syndrome comprises of epilepsy, ataxia, sensorineural deafness, and
tubulopathy. It is caused by a mutation in KCNJ10 gene. Less than thirty cases have been …

We encountered an extremely rare case where a patient with cat eye syndrome (CES) who
presented with symptoms of posterior semicircular canal dehiscence (PSCD). CES is a rare …

Objective Epilepsy surgery is widely accepted as an effective therapeutic option for carefully
selected patients with drug‐resistant epilepsy (DRE). There is limited data on the outcome …

… Ali Mir MD , Rami Alhazmi MD , Raidah Albaradie MD … Please cite this article as: Ali Mir
MD , Rami Alhazmi MD , Raidah Albaradie MD , Biotin-ThiamineResponsive Basal Ganglia …

Complete resolution of epileptic spasms with vigabatrin in a patient with 3-methylglutaconic
aciduria caused by TIMM50 gene mutation GLO: 8DU/01jul20: cge13763-toc-0001. jpg …

Absence of the cervical pedicle is a very rare congenital anomaly, easily misrecognized as
a unilateral facet dislocation in a setting of acute trauma or a neoplastic process like a nerve …

MEGDEL 3-methylglutaconic (MG) aciduria, deafness, encephalopathy, Leigh-like syndrome
is an autosomal recessive disorder associated with infantile hypoglycemia, progressive …

Our case involved a 1-year-old female with multiple admissions for chest infections. Given
her family history and high clinical suspicion, a diagnosis of Griscelli syndrome and …