Cystic fibrosis of pancreas and nephrotic syndrome: a rare association

Cystic fibrosis (CF) is a genetic disease with autosomal recessive inheritance and is common in Caucasian people. The prevalence of this disease is between 1/2,000 and 1/3,500 live births, and the incidence varies between populations. Although the CF transmembrane conductance regulator gene is expre...

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Main Authors: Selvi Kelekçi (Author), Müsemma Karabel (Author), Aydın Ece (Author), Velat Şen (Author), Ali Güneş (Author), İlyas Yolbaş (Author), Cahit Şahin (Author)
Format: Book
Published: Korean Pediatric Society, 2013-10-01T00:00:00Z.
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100 1 0 |a Selvi Kelekçi  |e author 
700 1 0 |a Müsemma Karabel  |e author 
700 1 0 |a Aydın Ece  |e author 
700 1 0 |a Velat Şen  |e author 
700 1 0 |a Ali Güneş  |e author 
700 1 0 |a İlyas Yolbaş  |e author 
700 1 0 |a Cahit Şahin  |e author 
245 0 0 |a Cystic fibrosis of pancreas and nephrotic syndrome: a rare association 
260 |b Korean Pediatric Society,   |c 2013-10-01T00:00:00Z. 
500 |a 1738-1061 
500 |a 2092-7258 
500 |a 10.3345/kjp.2013.56.10.456 
520 |a Cystic fibrosis (CF) is a genetic disease with autosomal recessive inheritance and is common in Caucasian people. The prevalence of this disease is between 1/2,000 and 1/3,500 live births, and the incidence varies between populations. Although the CF transmembrane conductance regulator gene is expressed in the kidneys, renal involvement is rare. With advances in the treatment of CF, life expectancy has increased, and some previously unobserved disease associations are now seen in patients with CF. It is important to follow patients with CF for possible abnormalities that may accompany CF. In this paper, we present two rare cases of CF accompanied by nephrotic syndrome. 
546 |a EN 
690 |a Cystic fibrosis 
690 |a Nephrotic syndrome 
690 |a Child 
690 |a Pediatrics 
690 |a RJ1-570 
655 7 |a article  |2 local 
786 0 |n Korean Journal of Pediatrics, Vol 56, Iss 10, Pp 456-458 (2013) 
787 0 |n http://kjp.or.kr/upload/pdf/kjped-56-456.pdf 
787 0 |n https://doaj.org/toc/1738-1061 
787 0 |n https://doaj.org/toc/2092-7258 
856 4 1 |u https://doaj.org/article/a27b4a9edf924b269d7ef76c33383d8d  |z Connect to this object online.