A 57-year-old male known case of diabetes mellitus presented with gradually bilateral decreased vision accompanied by ocular pain two weeks after SARS-CoV-2 infection. Ophthalmic examination and imaging were indicative of bilateral anterior ischemic optic neuropathy and secondary angle-closure glaucoma associated with increased choroidal thickness and hypercoagulable state following COVID-19 infection.

The present case report illustrates the rehabilitation of a 12-day old neonate with cleft palate. Since the palatal arch of the neonate was very small, a feeding spoon was innovatively modified to obtain the impression. The obturator was fabricated on the same day and delivered in one appointment.

Coronavirus disease is a viral infection affecting different organs with various morbidities and mortality. Vaccines are used to control the disease. COVID-19 vaccines have brought many benefits but their adverse effects should not be ignored. Here, we report a case of Guillain-Barré Syndrome Following Sinopharm COVID-19 Vaccine.

Rupture of ovarian dermoid-cyst is rare case. We report the case of a woman admitted for acute post-traumatic abdominal pain due to ruptured ovarian cyst. The patient was operated and we found a very abundant peritoneal effusion with left ovarian cyst which was broken. we performed a left adnexectomy.

Most instances of Guillain-Barré syndrome (GBS) are caused by immunological stimulation and are discovered after vaccinations for tetanus toxoid, oral polio, and swine influenza. This systematic study investigated GBS cases reported after receiving the COVID-19 vaccination.

Sneddon syndrome (SS) is a clinical entity corresponding to a non-inflammatory thrombotic vasculopathy that includes livedo reticularis (typical skin lesions) and cerebrovascular lesions. We present here a case of autoimmune SS with dementia and psychosis as the main features that revealed the disease, in a 45-year-old Tunisian man

Previous reports of clinical course of Angelman syndrome (AS) described typical histories of choking, dysphagia, and severe pneumonia, but there were few bedridden cases or none requiring laryngotracheal separation surgery (LTS) were existed. We report a severe bedridden case of AS requiring LTS involving a 19.3 Mb deletion on 15q11.2–q14.

A patient was referred to the oral medicine department with symptoms of redness and swelling of the lips and cheek, and intra-oral lesion. Biopsy was taken and laboratory factors were higher than normal, suggesting diagnosis of sarcoidosis. In this study we analyze the oral findings associated with sarcoidosis.

Terminal 11q deletion syndrome, also known as Jacobsen syndrome, is a rare genetic disorder. Children with Jacobsen syndrome have multiple risk factors for recurrent pneumonia. This is a case of recurrent pneumonia in a child with Jacobsen syndrome secondary to common variable immune deficiency.

A 78-year-old woman underwent surgical intervention for severe atrial functional mitral regurgitation and left ventricular apical aneurysm secondary to apical hypertrophic cardiomyopathy. Apical hypertrophic cardiomyopathy can cause atrial fibrillation and atrial functional mitral regurgitation. Left ventricular apical aneurysms can cause fatal arrhythmias, which may require surgical intervention.

Neurinomas are tumors of Schwann cells of the peripheral nerve sheath. Sacral location is rarely reported especially in spondyloarthritis patients. Herein, we report a case of uncommon pygalgia in a 25-year-old man with history of a non-radiographic axial spondyloarthritis and in whom the diagnosis of sacral neurinoma was established.

The emergent BPA, effective for even a central-type CTEPH, can lead the patient under fatal conditions to pulmonary endarterectomy.

Fixed drug eruption is a cutaneous drug reaction which recurs at the same site when the individual is exposed to the causative drug, characterized by single or multiple round sharply demarcated erythematous-to-violaceous patches. Here, we report a patient with generalized non-bullous fixed drug eruption following mRNA-based Pfizer-BioNTech COVID-19 vaccine.

Infraocclusion of a primary molar is a relatively common occurrence which seldom leads to serious complications, particularly when the succedaneous permanent tooth is present. Despite the relative infrequency of unfavourable outcomes, an infraoccluded primary molar may be associated with other dental anomalies, including hypodontia.

5 α reductase deficiency is a genetic disorder causing 46 XY disorder of sex development (DSD). Typical clinical feature is a male with female external genitalia or undervirilization at birth. Here we report 3 cases of this disorder within a family

We present a rare case of spontaneous osteodiscitis of the cervical spine complicated by epidural abscess/phlegmon, burst fracture, and spinal cord injury due to methicillin-resistant Staphylococcus aureus (MRSA) bacteremia in a patient with a history of intravenous drug use who presented with neck pain.

We report an extremely rare case of an ingrown nail with a subungual myiasis on the same toe in a female patient with no previous history of travel, trauma, contact with animals, immunosuppressive treatment or psychiatric disorders.

Aspiration thrombectomy is often performed in patients with acute myocardial infarction with high thrombus burden. Current guidelines, however, recommend against it because of stroke risk. We report a case of embolic stroke complicating coronary thrombus aspiration by an extremely rare mechanism.