enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Calcinosis cutis - Wikipedia

    en.wikipedia.org/wiki/Calcinosis_cutis

    Calcinosis cutis is an uncommon condition marked by calcium buildup in the skin and subcutaneous tissues. Calcinosis cutis can range in intensity from little nodules in one area of the body to huge, crippling lesions affecting a vast portion of the body. [ 1 ]

  3. Idiopathic scrotal calcinosis - Wikipedia

    en.wikipedia.org/wiki/Idiopathic_scrotal_calcinosis

    Idiopathic scrotal calcinosis is a cutaneous condition characterized by calcification of the skin resulting from the deposition of calcium and phosphorus occurring on the scrotum. [ 2 ] : 528 However, the levels of calcium and phosphate in the blood are normal. [ 3 ]

  4. Calcinosis - Wikipedia

    en.wikipedia.org/wiki/Calcinosis

    Calcinosis is the formation of calcium deposits in any soft tissue. [1] It is a rare condition that has many different causes. These range from infection and injury to systemic diseases like kidney failure .

  5. CREST syndrome - Wikipedia

    en.wikipedia.org/wiki/CREST_syndrome

    CREST syndrome, also known as the limited cutaneous form of systemic sclerosis (lcSSc), is a multisystem connective tissue disorder.The acronym "CREST" refers to the five main features: calcinosis, Raynaud's phenomenon, esophageal dysmotility, sclerodactyly, and telangiectasia.

  6. Dystrophic calcification - Wikipedia

    en.wikipedia.org/wiki/Dystrophic_calcification

    Calcinosis cutis is condition in which there are irregular nodular deposits of calcium salts in skin and subcutaneous tissue. Senile degenerative changes may be accompanied by calcification. The inherited disorder pseudoxanthoma elasticum may lead to angioid streaks with calcification of Bruch's membrane, the elastic tissue below the retinal ring.

  7. Familial hypocalciuric hypercalcemia - Wikipedia

    en.wikipedia.org/wiki/Familial_hypocalciuric...

    Familial hypocalciuric hypercalcemia (FHH) is an inherited condition that can cause hypercalcemia, a serum calcium level typically above 10.2 mg/dL; although uncommon. [1] It is also known as familial benign hypocalciuric hypercalcemia (FBHH) where there is usually a family history of hypercalcemia which is mild, a urine calcium to creatinine ratio <0.01, and urine calcium <200 mg/day ...

  8. Calciphylaxis - Wikipedia

    en.wikipedia.org/wiki/Calciphylaxis

    Calciphylaxis, also known as calcific uremic arteriolopathy (CUA) or “Grey Scale”, is a rare syndrome characterized by painful skin lesions.The pathogenesis of calciphylaxis is unclear but believed to involve calcification of the small blood vessels located within the fatty tissue and deeper layers of the skin, blood clots, and eventual death of skin cells due to lack of blood flow. [1]

  9. Calcification - Wikipedia

    en.wikipedia.org/wiki/Calcification

    Calcification can manifest itself in many ways in the body depending on the location. In the pulpal structure of a tooth, calcification often presents asymptomatically, and is diagnosed as an incidental finding during radiographic interpretation. Individual teeth with calcified pulp will typically respond negatively to vitality testing; te