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Related to hyalinosis: malalignment, transvesical
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7% with at least moderate arteriosclerosis) with or without intimal hyalinosis.
Devlin H, Sloan P, Thakkar NS: Oral manifastations of infantile systemic hyalinosis.
Urbach-Wiethe disease (lipoglycoproteinosis; lipoid proteinosis; hyalinosis cutis et mucosae).
Hypertension causes hyalinosis which disorganizes and disrupts the wall of the vessel resulting in thickening of the vessel wall and stenosis.
The glomeruli show a constellation of findings, including a diffuse form with mesangial sclerosis and uniform thickening of capillary loops, nodular lesions recognized as KW lesions, exudative or segmental hyalinosis lesions, and the subcapsular capsular drops.
Infantile systemic hyalinosis (ISH) is a rare genetic (CMG2) disorder caused by a mutation in the gene coding the protein responsible for the morphogenesis of capillary blood vessels (capillary morphogenetic protein 2) [Raham et al.
Lipoid proteinosis (Urbach-Wiethe disease, hyalinosis cutis et mucosae) is an autosomal-recessive condition with variable penetrance.
Throughout the tumor, there are changes represented by areas of hyalinosis, cystic degeneration, and lipidization.
In renal transplantation patients, arteriolar hyalinosis may be confused with amyloidosis because of the similar eosinophilic appearance.
In addition to the thrombi, the glomerular capillaries showed segmental areas of scarring, adhesion, and hyalinosis.
Although hyalinosis typically occurs in arterioles, similar changes can be seen in arteries.