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Cavalier King Charles Spaniel, a breed suspected to be predisposed to fly biting. Fly biting (also called fly catching or fly snapping) refers to a type of dog behavior: episodes of intentional focused biting at the air, as if the dog is biting at imaginary flies.
In psychology, relationship obsessive–compulsive disorder (ROCD) is a form of obsessive–compulsive disorder focusing on close and/or intimate relationships. [1] [2] Such obsessions can become extremely distressing and debilitating, having negative impacts on relationships functioning.
In general, use a potent preparation short term and weaker preparation for maintenance between flare-ups. While there is no proven best benefit-to-risk ratio, [11] if prolonged use of a topical steroid on a skin surface is required, a pulse therapy should be undertaken.
Benzodiazepine withdrawal syndrome (BZD withdrawal) is the cluster of signs and symptoms that may emerge when a person who has been taking benzodiazepines as prescribed develops a physical dependence on them and then reduces the dose or stops taking them without a safe taper schedule.
The term derives from Ancient Greek οὐροβόρος, [6] from οὐρά oura 'tail' plus -βορός-boros '-eating'. [7] [8]The ouroboros is often interpreted as a symbol for eternal cyclic renewal or a cycle of life, death and rebirth; the snake's skin-sloughing symbolises the transmigration of souls.
Joseph Carey Merrick (5 August 1862 – 11 April 1890), often erroneously called John Merrick, was an English artist known for his severe physical deformities.He was first exhibited at a freak show under the stage name "the Elephant Man", and then went to live at the London Hospital, in Whitechapel, after meeting Sir Frederick Treves, subsequently becoming well known in London society.
Paronychia is an inflammation of the skin around the nail, which can occur suddenly (acute), when it is usually due to the bacterium Staphylococcus aureus, or gradually (chronic) when it is commonly caused by Candida albicans.
Lesch–Nyhan syndrome (LNS) is a rare inherited disorder caused by a deficiency of the enzyme hypoxanthine-guanine phosphoribosyltransferase (HGPRT). This deficiency occurs due to mutations in the HPRT1 gene located on the X chromosome.