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A Case Report on A Rare Disease: Isolated Renal Glucosuria

Yıl 2023, Cilt: 1 Sayı: 3, 103 - 104, 31.10.2023

Öz

Isolated renal glucosuria is defined as urinary excretion of glucose when the blood glucose level is normal. It is a rare and benign disease. The majority of the cases are asymptomatic. Most cases of isolated glycosuria, which are diagnosed by complete urinalysis and exclusion of other diseases that cause glycosuria, are followed up without treatment. Diabetes mellitus must be excluded before the diagnosis of isolated renal glucosuria. In this article, we presented a case who did not have any symptoms and underwent diagnostic evaluation due to glycosuria.

Kaynakça

  • Scholl-Bürgi S, Santer R, Ehrich JH. Long-term outcome of renal glucosuria type 0: the original patient and his natural history. Nephrol Dial Transplant. 2004;19:2394-6.
  • Calado J, Loeffler J, Sakallioglu O, et al. Familial renal glucosuria: SLC5A2 mutation analysis and evidence of salt-wasting. Kidney Int. 2006;69:852-5.
  • Magen D, Sprecher E, Zelikovic I, et al. A novel missense mutation in SLC5A2 encoding SGLT2 underlies autosomal-recessive renal glucosuria and aminoaciduria. Kidney Int. 2005;67:34- 41.
  • Francis J, Zhang J, Farhi A, et al. A novel SGLT2 mutation in a patient with autosomal recessive renal glucosuria. Nephrol Dial Transplant. 2004;19:2893-5.
  • Calado J, Soto K, Clemente C, Correia P, Rueff J. Novel compound heterozygous mutations in SLC5A2 are responsible for autosomal recessive renal glucosuria. Hum Genet. 2004;114:314- 6.
  • Dönmez O, Köse H. Çocuklarda Renal glukozüri. Güncel Pediatri. 2004;2:134-6.
  • Wu CJ. Transient renal glycosuria in a patient with acute pyelonephritis. Intern Med. 2001;40:519-21.
  • Sodeman, W.A, Sodeman, T.M.: Sodeman’s Pathologic Physiology, Mechanisms of disease, W.B, Saunders Co., Philadelphia, 6 th Ed. 1979;415:87.

Nadir Bir Hastalık: İzole Renal Glukozüri

Yıl 2023, Cilt: 1 Sayı: 3, 103 - 104, 31.10.2023

Öz

İzole renal glukozüri, kan glukoz seviyesinin normal olduğu durumlarda glukozun idrar yoluyla atılması olarak tanımlanmaktadır. Nadir ve benign karakterli bir hastalıktır. Olguların çoğu semptom vermemektedir. Tam idrar tetkik sonucu ve diğer glukozüri yapan hastalıkların dışlanması ile teşhis alan izole glukozüri olguların çoğu tedavi edilmeksizin takibe alınmaktadır. İzole renal glukozüri tanısı öncesi mutlaka diyabetes mellitus dışlanması şarttır. Bu yazımızda herhangi bir semptomu olmayan ve glukozüri nedeniyle tanısal değerlendirilmesi yapılan olguyu sunuyoruz.

Kaynakça

  • Scholl-Bürgi S, Santer R, Ehrich JH. Long-term outcome of renal glucosuria type 0: the original patient and his natural history. Nephrol Dial Transplant. 2004;19:2394-6.
  • Calado J, Loeffler J, Sakallioglu O, et al. Familial renal glucosuria: SLC5A2 mutation analysis and evidence of salt-wasting. Kidney Int. 2006;69:852-5.
  • Magen D, Sprecher E, Zelikovic I, et al. A novel missense mutation in SLC5A2 encoding SGLT2 underlies autosomal-recessive renal glucosuria and aminoaciduria. Kidney Int. 2005;67:34- 41.
  • Francis J, Zhang J, Farhi A, et al. A novel SGLT2 mutation in a patient with autosomal recessive renal glucosuria. Nephrol Dial Transplant. 2004;19:2893-5.
  • Calado J, Soto K, Clemente C, Correia P, Rueff J. Novel compound heterozygous mutations in SLC5A2 are responsible for autosomal recessive renal glucosuria. Hum Genet. 2004;114:314- 6.
  • Dönmez O, Köse H. Çocuklarda Renal glukozüri. Güncel Pediatri. 2004;2:134-6.
  • Wu CJ. Transient renal glycosuria in a patient with acute pyelonephritis. Intern Med. 2001;40:519-21.
  • Sodeman, W.A, Sodeman, T.M.: Sodeman’s Pathologic Physiology, Mechanisms of disease, W.B, Saunders Co., Philadelphia, 6 th Ed. 1979;415:87.
Toplam 8 adet kaynakça vardır.

Ayrıntılar

Birincil Dil Türkçe
Konular İç Hastalıkları
Bölüm Olgu Sunumu
Yazarlar

Uğur Ergün 0000-0002-6111-0030

Yayımlanma Tarihi 31 Ekim 2023
Gönderilme Tarihi 22 Ağustos 2023
Yayımlandığı Sayı Yıl 2023 Cilt: 1 Sayı: 3

Kaynak Göster

AMA Ergün U. Nadir Bir Hastalık: İzole Renal Glukozüri. Ağrı Med J. Ekim 2023;1(3):103-104.