Epidermolysis Bullosa (EB) is a rare heritable disease of the skin, manifests at birth, early childhood, or adults with different subtypes (simplex, recessive, dystrophic, and junctional) that cannot be separated clinically.
Published on 20 Nov, 2020
We report the case of a 37-year-old woman with vulvar squamous cell carcinoma, status post bilateral vulvectomy with lymph node dissection.
Published on 16 Nov, 2020
Bite infections caused by Capnocytophaga canimorsus are rare.
Published on 06 Nov, 2020
Esophageal perforation due to foreign body usually presents clinically with severe pain occurring within hours of the insult.
Published on 29 Oct, 2020
Introduction: NOMID/CINCA Syndrome (Neonatal Onset Multisystem Inflammatory Disease/Chronic Infantile Neurologic Cutaneous and Articular Syndrome) is a rare inflammatory periodic fever syndrome responding to treatment with IL-1 antagonists.
Published on 23 Oct, 2020
Purpose: This case report discusses a case of unilateral ocular mass and migraine headaches in a 28-year-old female who was referred to the retina service.
Published on 23 Oct, 2020
A 78-year-old Hispanic female with a past medical history of cryptogenic cirrhosis with ascites and congestive heart failure presented to the emergency department with abdominal pain after a fall.
Published on 16 Oct, 2020
Ankyloblepharon Filiforme Adnatum (AFA) is a benign rare congenital disorder of the eyelid.
Published on 15 Oct, 2020
Background: Bradycardia during weaning from Mechanical Ventilation (MV) and Pressure Support Ventilation (PSV) is a rare occurrence, with only one such case report found in the literature.
Published on 08 Oct, 2020
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