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Çocukluk Çağı Sistin Taşı ve Sistinüri

Year 1997, Volume: 2 Issue: 1, 34 - 35, 30.01.1997

Abstract

Çocukluk döneminde sistin taş oluşumu nadirdir. Bu
makalede 1 yaşındaki sistin taşlı olgu sunulmuş ve ilgili literatür gözden
geçirilmiştir. Akrabalar arası evliliklerin sık olduğu ülkemizde, pek çoğu
otozomal resesif yolla geçen metabolik hastalıklara sıkça rastlanılmaktadır. Bu
nedenle üriner sistemde taş tespit edilen olguların, özellikle de çocukların,
metabolik yönden de araştırılması yerinde olacaktır.

References

  • Thier SO, Segal S: Cystinuria. İçinde: Stonbury JB. Wyngaarden JB, Frederickson DS, ed. The Metabolic Basis of Inherited Dease. New York: McGraw-Hill Book Co; 1972:1504-1514.
  • Pak CYC. Cystine lithiasis. İçinde: Resnick MI, Pak CYC, ed. Urolithiasis. Philadelphia: W.B. Saunders Comp; 1990:133-143.
  • Eckstein HB. Endemic urinary lithiasis in Turkish children. Arch Dis Child. 1961;36:127-130.
  • Gültekin A, Özalp İ, Tanzer F, Hasanoğlu A. Türk çocuklarında sistinürinin görülme sıklığı (20 gün-20 yaş arasında 8572 olgunun tarama sonuçları). Çocuk Sağlığı ve Hastalıkları Dergisi. 1980;23:1-8.
  • Polinsky MS, Kaiser BA, Baluarte HJ. Urolithiasis in childhood. Pediatr. Clin. North Am. 1987;34(3):683-710. doi:10.1016/s0031-3955(16)36262-9
  • Pruzanski W. Cystinuria and cystine urolithiasis in childhood. Acta Paediatr. Scan. 1966;55:97-106. doi:10.1111/j.1651-2227.1966.tb15214.x
  • Evans WP, Resnick MI, Boyce WH. Homozygous cystinuria: Evaluation of 35 patients. J. Urol. 1982;127:707-709. doi:10.1016/S0022-5347(17)54007-0
  • Yeh HL, Frankl W, Dunn MS. The urinary excretion of amino acids by cystinuric subjects. Am. J. Med. Sci. 1967;214:507-514.

Cystinuria and Cystine Lithiasis in Childhood

Year 1997, Volume: 2 Issue: 1, 34 - 35, 30.01.1997

Abstract

In childhood, cystine urolithiasis is rare. We
presented a one-year-old child with cystine urolithiasis and reviewed the
literature. In our population, as the marriages among relatives are common, the
incidence of autosomal recessive diseases are quite high. So, if there is a
recognized urolithiasis in a child, it should be researched for a possible
metabolic disorder.

References

  • Thier SO, Segal S: Cystinuria. İçinde: Stonbury JB. Wyngaarden JB, Frederickson DS, ed. The Metabolic Basis of Inherited Dease. New York: McGraw-Hill Book Co; 1972:1504-1514.
  • Pak CYC. Cystine lithiasis. İçinde: Resnick MI, Pak CYC, ed. Urolithiasis. Philadelphia: W.B. Saunders Comp; 1990:133-143.
  • Eckstein HB. Endemic urinary lithiasis in Turkish children. Arch Dis Child. 1961;36:127-130.
  • Gültekin A, Özalp İ, Tanzer F, Hasanoğlu A. Türk çocuklarında sistinürinin görülme sıklığı (20 gün-20 yaş arasında 8572 olgunun tarama sonuçları). Çocuk Sağlığı ve Hastalıkları Dergisi. 1980;23:1-8.
  • Polinsky MS, Kaiser BA, Baluarte HJ. Urolithiasis in childhood. Pediatr. Clin. North Am. 1987;34(3):683-710. doi:10.1016/s0031-3955(16)36262-9
  • Pruzanski W. Cystinuria and cystine urolithiasis in childhood. Acta Paediatr. Scan. 1966;55:97-106. doi:10.1111/j.1651-2227.1966.tb15214.x
  • Evans WP, Resnick MI, Boyce WH. Homozygous cystinuria: Evaluation of 35 patients. J. Urol. 1982;127:707-709. doi:10.1016/S0022-5347(17)54007-0
  • Yeh HL, Frankl W, Dunn MS. The urinary excretion of amino acids by cystinuric subjects. Am. J. Med. Sci. 1967;214:507-514.
There are 8 citations in total.

Details

Primary Language Turkish
Subjects Paediatrics
Journal Section Research Articles
Authors

A. Sıtkı Özdamar This is me

Esra Baskın This is me

Sadi Turkan This is me

Ali Gökalp This is me

Publication Date January 30, 1997
Submission Date September 1, 1996
Acceptance Date January 1, 1997
Published in Issue Year 1997 Volume: 2 Issue: 1

Cite

AMA Özdamar AS, Baskın E, Turkan S, Gökalp A. Çocukluk Çağı Sistin Taşı ve Sistinüri. Acta Med Nicomedia. January 1997;2(1):34-35.

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