Oxalosis in an inherited disease characterized by growth retardation recurrent urolithiasis nephrocalcinosis renal failure and deposition of oxalates in the tissues Type I is the most common from seen in early childhood on the other hand in type II LGlyceric acid is high in urine besides hyperoxaluria A 75 month old girl was admitted with growth retardation Her renal functions were impaired and bilateral nephrocalcinosis was observed by renal ultrasonography Although peritoneal dialysis was performed immediately the patient died and necropsy findings showed crystalloid deposition in the kidney Key words: Oxalosis Nephrocalcinosis Treatment
📌 3 Key Takeaways
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Objective & Hypothesis:Oxalosis in an inherited disease characterized by growth retardation recurrent urolithiasis nephrocalcinosis renal failure and deposition of oxalates in the tissues Type I is the most common from seen in early childhood on the other hand in type II LGlyceric acid is high in urine besides hyperoxaluria A 75 month old girl was admitted with growth retardation Her renal functions were impaired and bilateral nephrocalcinosis was observed by renal ultrasonography Although peritoneal dialysis was performed immediately the patient died and necropsy findings showed crystalloid deposition in the kidney Key words: Oxalosis Nephrocalcinosis Treatment
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Key Findings & Data:Oxalosis in an inherited disease characterized by growth retardation recurrent urolithiasis nephrocalcinosis renal failure and deposition of oxalates in the tissues Type I is the most common from seen in early childhood on the other hand in type II LGlyceric acid is high in urine besides hyperoxaluria A 75 month old girl was admitted with growth retardation Her renal functions were impaired and bilateral nephrocalcinosis was observed by renal ultrasonography Although peritoneal dialysis was performed immediately the patient died and necropsy findings showed crystalloid deposition in the kidney Key words: Oxalosis Nephrocalcinosis Treatment
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Conclusion & Impact:Oxalosis in an inherited disease characterized by growth retardation recurrent urolithiasis nephrocalcinosis renal failure and deposition of oxalates in the tissues Type I is the most common from seen in early childhood on the other hand in type II LGlyceric acid is high in urine besides hyperoxaluria A 75 month old girl was admitted with growth retardation Her renal functions were impaired and bilateral nephrocalcinosis was observed by renal ultrasonography Although peritoneal dialysis was performed immediately the patient died and necropsy findings showed crystalloid deposition in the kidney Key words: Oxalosis Nephrocalcinosis Treatment
🔬Design:Makale
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters
Abstract
Oxalosis in an inherited disease characterized by growth retardation recurrent urolithiasis nephrocalcinosis renal failure and deposition of oxalates in the tissues Type I is the most common from seen in early childhood on the other hand in type II LGlyceric acid is high in urine besides hyperoxaluria A 75 month old girl was admitted with growth retardation Her renal functions were impaired and bilateral nephrocalcinosis was observed by renal ultrasonography Although peritoneal dialysis was performed immediately the patient died and necropsy findings showed crystalloid deposition in the kidney Key words: Oxalosis Nephrocalcinosis Treatment
Özet
Primer hiperoksalüri; hiperoksalüri içeriği kalsiyum oksalat olan ürolitiasis nefrokalsinoz ve erken dönemde böbrek yetersizliği ile karakterize otosomal resessif geçişli nadir bir metabolik hastalıktır Olguların çoğunluğu çocukluk döneminde ilk 5 yaşta renal semptomlar verir İki ayrı tipi vardır Tip I ve II Kalsiyum oksalat birikimleri böbrek dışında diğer dokularda da gözlenebilir Bu duruma oksalosis denilir Aşağıda infantil dönemde nefrokalsinoza yol açan bir olgu sunulmaktadır Anahtar kelimeler: Oksalosis Nefrokalsinoz Tedavi
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Cite This Article
Ünüvar, A., Nayır, A., Alpay, H., Uysal, V., Emre, S., Şirin, A., Tanman, F., Çubukçu, O. (1993). A Rare Cause of Nephrocalcinosis in Childhood: Oxalosis. Türk Pediatri Arşivi, Cilt: 28 Sayı: 1. https://ajindex.com/articles/1438124