Background: Osteogenesis imperfecta (OI), also known as brittle bone disease, is a rare genetic multisystem disorder of Type I collagen associated with bone fragility, fractures and connective tissue abnormalities, with highly heterogeneous phenotypic features and varying genetic...
Open access
Research Article10.9734/ajcrs/2026/v9i2820
Kamli Abderrahim, Ayoub Boutahar, Othmane Alaoui, Abdelhalim Mahmoudi, Khalid Khattala & Youssef Bouabdallah·Asian Journal of Research in Surgery·2026
Background: Oesophageal achalasia (EA) is a rare primary motility disorder of the oesophagus characterised by absent oesophageal peristalsis and incomplete relaxation of the lower oesophageal sphincter (LES). In children, diagnosis is frequently delayed because of an atypical and...
Open access
Research Article10.9734/ajrs/2026/v9i2396
Introduction: Chronic bacterial osteitis is a rare inflammatory disease in children that can mimic certain tumor lesions, particularly eosinophilic granuloma. Forms localized to a single site, particularly at the lower end of the radius, are uncommon and make the diagnosis diffic...
Open access
Research Article10.9734/ajcrs/2026/v9i1733
Introduction: Osteochondromas are the most common benign bone tumors, but their scapular location, particularly on the anterior surface, remains exceptional. They may reveal themselves through unusual clinical or radiological presentation. Observation: We report the case of a 13-...
Open access
Research Article10.9734/ajcrs/2025/v8i2710