Results 81 to 90 of about 2,548 (196)
International Journal of Nephrology, 2011 Primary hyperoxalurias (PH) are inborn errors in the metabolism of glyoxylate and oxalate. PH type 1, the most common form, is an autosomal recessive disorder caused by a deficiency of the liver-specific enzyme alanine, glyoxylate aminotransferase (AGT ...
Jérôme Harambat +4 more
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Oral manifestations of oxalosis: A case report and review of the literature
, 2008 Primary hyperoxaluria (PH) is a metabolic autosomal recessive disease that causes an error in oxalate metabolism. In 1957, Archer et al(1) introduced the term primary hyperoxaluria. Two types are known.
Oosterhuis, Wolter +3 more
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International Journal of Nephrology, 2011 A 29-year old female presented with a one-week history of vomiting, diarrhoea, abdominal pain, and headache. On admission, she had acute renal failure requiring dialysis. Tests revealed a hemolytic anemia with thrombocytopenia.
Karolina M. Stepien +4 more
doaj +1 more source
, 2018 Primary hyperoxaluria type 1 (PH1) is a rare life-threatening genetic disease related to glyoxylate metabolism and characterized by accumulation of calcium oxalate crystals.
Moya-Garzón, María Dolores +8 more
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Aspergillus Niger Infection Associated with Systemic Oxalosis: An Autopsy Diagnosis Without Culture
, 2014 This case report presents a 60-year-old male with a past medical history that included diabetes mellitus type II, chronic alcoholism, Hepatitis C infection, and presumptive pneumonia who died following a cholecystectomy.
Albert Jenkins +2 more
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Isolated Nasopharyngeal Aspergillosis Caused by A flavus and Associated with Oxalosis
, 2004 We report a case of isolated nasopharyngeal aspergillosis in a 52-year-old woman with Hashimoto's thyroiditis. We found the nasopharyngeal lesion incidentally while evaluating bilateral cervical lymphadenopathy, which we had discovered during a ...
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, 2015 Hyperoxaluria type I (HPI) is a metabolic disorder secondary to liver alanine glyoxylate aminotransferase deficiency. Renal failure occurs due to the excessive production and precipitation of oxalate in the kidney. Combined liver-renal transplantation is
Sinangil A. +5 more
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Liver-Kidney Transplantation in Primary Hyperoxaluria Type-1: Case Report and Literature Review
International Journal of Organ Transplantation Medicine, 2011 Primary hyperoxaluria type-1 (PH1) is a rare inherited autosomal recessive disorder in which a deficiency of the hepatic enzyme alanine-glyoxylate aminotransferase leads to endogenous oxalate overproduction, renal failure, systemic oxalate deposition and
D Siegal +5 more
doaj
Cutaneous oxalosis is an uncommon manifestation of primary hyperoxalosis, which can often resemble other cutaneous manifestations of end stage renal disease (ESRD), particularly calciphylaxis.
Kaci Reaves +3 more
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