نتایج جستجو برای: hyalinosis

تعداد نتایج: 1670  

2014
Seyed Reza Raeeskarami Yahya Aghighi Azadeh Afshin Abdolreza Malek Ali Zamani Vahid Ziaee

BACKGROUND Infantile Systemic Hyalinosis (ISH) is a very rare autosomal recessive disorder characterized by connective tissue involvement as hyaline deposition in skin, gastrointestinal tract, muscles, glands and other organs. CASES PRESENTATION We report eight Iranian children (4 male and 4 female) with ISH referred to our hospital from 1996 to 2013. The illness had been diagnosed by clinica...

Journal: :Oman medical journal 2013
Siham Al Sinani Fathyia Al Murshedy Reem Abdwani

Infantile Systemic Hyalinosis (ISH) (OMIM 236490) is a rare, progressive and fatal autosomal recessive disorder characterized by multiple subcutaneous skin nodules, gingival hypertrophy, osteopenia, joint contractures, failure to thrive, diarrhea with protein losing enteropathy, and frequent infections. There is diffuse deposition of hyaline material in the skin, gastrointestinal tract, muscle ...

Journal: :Archivos argentinos de pediatria 2015
Diego Alejandro Rangel Rivera Víctor Clemente Mendoza Rojas Claudia Janeth Uribe Pérez Gustavo Adolfo Contreras-García

Hyaline fibromatosis syndrome is a rare autosomal recessive disease characterized by the presence of contracture and joint pain, hyperpigmented plaques and nodules and gingival hypertrophy. These findings are the result of the accumulation of a hyaline amorphous material similar to collagen type VI in different tissues. This syndrome includes systemic hyalinosis and juvenile hyaline fibromatosi...

Journal: :Sri Lanka Journal of Child Health 2023

No abstract available Sri Lanka Journal of Child Health, 2023: 52(2): 223-227

Journal: :Open journal of nephrology 2023

Introduction: Focal Segmental Glomerulosclerosis (FSGS) corresponds to a clinicopathological syndrome, manifested by generally abundant proteinuria associated with hyaline deposits on part of certain glomeruli and sparing other glomeruli, effacement the pedicels. The general objective was determine prevalence FSGS, give its profiles; epidemiological, clinical, biological, pathological, etiologi...

Journal: :Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2010
Agnes B Fogo Leif Bostad Einar Svarstad William J Cook Solange Moll Federic Barbey Laurette Geldenhuys Michael West Dusan Ferluga Bojan Vujkovac Alexander J Howie Aine Burns Roy Reeve Stephen Waldek Laure-Hélène Noël Jean-Pierre Grünfeld Carmen Valbuena João Paulo Oliveira Justus Müller Frank Breunig Xiao Zhang David G Warnock

BACKGROUND In Fabry nephropathy, alpha-galactosidase deficiency leads to accumulation of glycosphingolipids in all kidney cell types, proteinuria and progressive loss of kidney function. METHODS An international working group of nephrologists from 11 Fabry centres identified adult Fabry patients, and pathologists scored histologic changes on renal biopsies. A standardized scoring system was d...

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