Search results
Results From The WOW.Com Content Network
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 ]
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 ]
Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Donate
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.
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 .
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.
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]
Calcinosis cutis; Carotenoderma; Carotenosis; Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy syndrome; Cerebrotendinous xanthomatosis; Chylomicronemia; Chylomicronemia syndrome; Citrullinemia; Combined hyperlipidemia; Congenital erythropoietic porphyria