List of articles in "Disease" category - Page 516

Ototoxicity is the quality of being toxic to the ear (oto-) specifically the cochlea or auditory nerve and sometimes the vestibular system; it is commonly medication-induced. Ototoxic drugs include antibiotics […]

A stabbing is penetration with a sharp or pointed object at close range. Stab connotes purposeful action as by an assassin or murderer but it is also possible to accidentally […]

Epidermolytic hyperkeratosis (also known as Bullous congenital ichthyosiform erythroderma Bullous ichthyosiform erythroderma or bullous congenital ichthyosiform erythroderma Brocq) is a rare ichthyosis skin disease affecting around 1 in 250000 people.It […]

Lamellar ichthyosis also known as ichthyosis lammellaris and nonbullous congenital ichthyosis is a rare inherited skin disorder affecting around 1 in 600000 people.

Ichthyosis vulgaris (also known as Autosomal dominant ichthyosis and Ichthyosis simplex) is a skin disorder causing dry scaly skin. It is the most common form of ichthyosis affecting around 1 […]

In medicine inflammatory bowel disease (IBD) is a group of inflammatory conditions of the colon and small intestine. The major types of IBD are Crohn’s disease and ulcerative colitis.

Waardenburg syndrome (also Waardenburg­ Shah Syndrome Waardenburg-Klein syndrome Mende’s syndrome II Van der Hoeve-Halbertsma-Waardenburg syndrome Ptosis-Epicanthus syndrome Van der Hoeve-Halbertsma-Gualdi syndrome Waardenburg type Pierpont[5] Van der Hoeve-Waardenburg-Klein syndrome Waardenburg’s syndrome […]

In anatomy heterochromia (Greek: heteros ‘different’ + chroma ‘color’) is a difference in coloration usually of the iris but also of hair or skin. Heterochromia is a result of the […]

Frenulum breve or a short frenulum is a condition in which the frenulum preputii penis which is an elastic band of tissue under the glans penis that connects to the […]

Fabry disease (/ˈfɑːbri/) (also known as Fabry’s disease Anderson-Fabry disease angiokeratoma corporis diffusum and alpha-galactosidase A deficiency) is a rare genetic lysosomal storage disease inherited in an X-linked manner. Fabry […]