Sturge–Weber syndrome sometimes referred to as encephalotrigeminal angiomatosis is a rare congenital neurological and skin disorder. It is one of the phakomatoses and is often associated with port-wine stains of […]
List of articles in "Disease" category - Page 397
Primary progressive aphasia
Primary progressive aphasia (PPA) is characterized by progressive language and speech disorders. It was first described as a distinct syndrome by Mesulam in 1982.
Patellar tendinitis
Patellar tendinitis (patellar tendinopathy also known as jumper’s knee) is a relatively common cause of pain in the inferior patellar region in athletes. It is common with frequent jumping and […]
Valvular heart disease
Valvular heart disease is any disease process involving one or more of the four valves of the heart (the aortic and mitral valves on the left and the pulmonary and […]
Corneal abrasion
For corneal abrasions in dogs and cats see Corneal ulcers in animals.Corneal abrasion is a medical condition involving the loss of the surface epithelial layer of the eye’s cornea.
Congenital lacrimal duct obstruction
Congenital nasolacrimal duct obstruction (CLDO) is the condition in which a tear duct has failed to open at the time of birth. Around 6% of infants have CLDO usually experiencing […]
Recurrent corneal erosion
Recurrent corneal erosion is a disorder of the eyes characterized by the failure of the cornea’s outermost layer of epithelial cells to attach to the underlying basement membrane (Bowman’s layer). […]
Female genital prolapse
Female genital prolapse (or vaginal prolapse or pelvic organ prolapse) is characterized by a portion of the vaginal canal protruding (prolapsing) from the opening of the vagina. The condition usually […]
GM2-gangliosidosis AB variant
GM2-gangliosidosis AB variant is a rare autosomal recessive metabolic disorder that causes progressive destruction of nerve cells in the brain and spinal cord. It has a similar pathology to Sandhoff […]
Carnitine palmitoyltransferase II deficiency
Carnitine palmitoyltransferase II deficiency (CPT-II) is a metabolic disorder characterized by an enzymatic defect that prevents long-chain fatty acids from being transported into the mitochondria for utilization as an energy […]