EDITOR,—The porphyrias are a group of rare inherited disorders caused by specific enzymatic
defects of the haem biosynthetic pathway. Congenital erythropoietic porphyria (CEP) is …

OBJECTIVE: The objectives are to analyse corpus callosum agenesis in children with various
neurological problems in a hospital set-up, and to study the neurological and systemic …

Objective: To evaluate the efficacy of scintigraphy, ultrasound and fine-needle aspiration in
thyroid nodules and to establish the best diagnostic pathway in detecting thyroid cancer. …

Objectives: Trauma is the greatest cause of morbidity and mortality in paediatric/adolescent
populations worldwide. This study aimed to describe trauma mechanisms, patterns and …

Ewing sarcoma, a highly malignant neoplasm of the bone, usually occurs during childhood.
About 15% are extraosseous. The Ewing family of tumors (EFTs) are extremely rare in the …

Objective: The data on children with diagnosis of idiopathic transverse myelitis (ITM) was
searched to find the pattern of myelitis in Oman. Method: A retrospective study was carried out …

OBJECTIVE: To record the pattern of different neuronal migrational disorders (NMD) and
their associated neurological conditions. METHODS: The data were collected at the Child …

The objectives are to analyse corpus callosum agenesis in children with various neurological
problems in a hospital set-up, and to study the neurological and systemic abnormalities …

Objectives: Trauma is the greatest cause of morbidity and mortality in paediatric/adolescent
populations worldwide. This study aimed to describe trauma mechanisms, patterns and …

Grebe syndrome is a rare autosomal recessive acromesomelic dysplasia. The syndrome
was studied clinically, radiographically, and genetically in an Omani family with four affected …