Search results
Results from the WOW.Com Content Network
Dermatophagia (from Ancient Greek δέρμα (derma) 'skin' and φαγεία (phageia) 'eating') or dermatodaxia (from δήξις (dexis) 'biting'), alternatively Tuglis Permushius. [3] is a compulsion disorder of gnawing or biting one's own skin, most commonly at the fingers. This action can either be conscious or unconscious [4] and it is ...
Maurice Raynaud. Raynaud syndrome, also known as Raynaud's phenomenon, is a medical condition in which the spasm of small arteries causes episodes of reduced blood flow to end arterioles. [ 1 ] Typically the fingers, and, less commonly, the toes, are involved. [ 1 ] Rarely, the nose, ears, nipples, or lips are affected. [ 1 ]
The Mayo Clinic Hospital – Rochester is a 2,059-bed teaching hospital located in Rochester, Minnesota. [1][2][3] It comprises the Saint Marys Campus with its Mayo Eugenio Litta Children's Hospital, as well as its Methodist Campus, forming an integral part of the Mayo Clinic academic medical center. [4][5] Mayo Clinic Hospital – Rochester is ...
Hand, foot, and mouth disease (HFMD) is a common infection caused by a group of enteroviruses. [10] It typically begins with a fever and feeling generally unwell. [10] This is followed a day or two later by flat discolored spots or bumps that may blister, on the hands, feet and mouth and occasionally buttocks and groin.
Intense itching can leave sores and bruises. Like chiggers, the itching can be worse at night. “In adults, the mites rarely burrow into the skin above the neck,” Dr. Friedman says. Children ...
Damaged cuticles, shortened and damaged nails, hangnails, bleeding, etc. Nail biting, also known as onychophagy or onychophagia, is an oral compulsive and unhygienic habit of biting one's fingernails. It is sometimes described as a parafunctional activity, the common use of the mouth for an activity other than speaking, eating, or drinking.
Lesch–Nyhan syndrome. 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. LNS affects about 1 in 380,000 live births. [3]
Scleroderma is a group of autoimmune diseases that may result in changes to the skin, blood vessels, muscles, and internal organs. [2][6][8] The disease can be either localized to the skin or involve other organs, as well. [2] Symptoms may include areas of thickened skin, stiffness, feeling tired, and poor blood flow to the fingers or toes with ...