Zoon Balanitis
Eponym Zoon's balanitis, ie balanitis chronica circumscripta plasmacellularis. Johannes Jacobus Zoon (1902-1958) was a Dutch dermatologist.
Category Eponymictionary
Essex-Lopresti fracture
Essex-Lopresti injury consists of a radial head fracture AND dislocation of the distal radioulnar joint (DRUJ) AND disruption of the interosseous membrane (IOM)
Forestier disease
Diffuse idiopathic skeletal hyperostosis (DISH), the now more generally accepted name for Forestier disease; is a poorly understood, systemic condition characterised by progressive calcification and ossification of ligaments and entheses
Emil Naclerio
Emil Anthony Naclerio (1915-1985) was an Italian-American Thoracic Surgeon. Naclerio's V sign in oesophageal rupture
Mondor disease
Mondor disease is a rare, benign condition characterized by thrombophlebitis of the subcutaneous veins of the breast and anterolateral chest wall.
Penile Mondor disease
Penile Mondor’s disease (PMD) is an isolated superficial thrombophlebitis of the superficial dorsal vein of the penis.
Bazett formula
Bazett formula 'corrects' the measured QT interval to a value (QTc) attributable to a heart rate of 60 bpm. Thus providing a QT interval value that a particular patient would theoretically have if their heart rate was 60 beats/min
Fridericia Formula
Fridericia Formula for calculating the QT interval on an (ECG) according to heart rate, described in 1920. Louis Sigurd Fridericia (1881-1947)
Da Costa Syndrome
Da Costa syndrome (soldier's heart, neurocirculatory asthenia) most commonly considered a manifestation of an anxiety disorder
Chance fracture
Chance fracture is a transverse fracture through a vertebral body and neural arch. Described by George Quentin Chance, British radiologist in 1948
Baastrup disease
Baastrup sign (kissing spines) refers to an orthopaedic condition / radiological sign with enlargement and approximation of adjacent spinous processes with normal intervertebral disc height and neuroforamina
Albers-Schönberg disease
Albers-Schönberg disease is the most common form of osteopetrosis. Also known as autosomal dominant osteopetrosis type II (ADO II)