Journals / Turkish Journal of Gastroenterology / 2017 / Cilt: 28 - Sayı: 6

Surgical consequences in infants with delayed diagnosis of congenital chloride diarrhea

Pages
510–513
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Here we describe five such cases

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Despite the usual typical presentation, congenital chloride diarrhea (CCD) poses multiple diagnostic challenges.
📊
Key Findings & Data:It has an incidence of 1/5000 in Saudi Arabia.
💡
Conclusion & Impact:Here we describe five such cases
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Özet

Despite the usual typical presentation, congenital chloride diarrhea (CCD) poses multiple diagnostic challenges. It has an incidence of 1/5000 in Saudi Arabia. CCD can mimic intestinal obstruction and result in avoidable surgical interventions. Contributing factors are abdominal distension and the watery (urine-like) diarrhea that is often interpreted as delayed passage of meconium. Surgical interventions would unnecessarily increase the morbidity. Therefore, a high index of suspicion and educating neonatologists, general pediatricians, and pediatric surgeons regarding this diagnostic entity is essential. Here we describe five such cases

🔖

Cite This Article

AWADHİ, H. A., MEHAİDİB, A. A., ALSALEEM, K., BANEMAİ, M., DEKHAİL, W. A. (2017). Surgical consequences in infants with delayed diagnosis of congenital chloride diarrhea. Turkish Journal of Gastroenterology, Cilt: 28 - Sayı: 6, 510–513. https://ajindex.com/articles/410714

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (14)

  1. Seo KA, Lee NM, Kim GJ, et al. Congenital chloride diarrhea in dizygotic twins. Pediatr Gastroenterol Hepatol Nutr 2013; 16: 195-9
  2. Alzahrani AK. Congenital chloride losing diarrhea. Pediatr Ther 2014; 4: 193
  3. Özbay Hoşnut F, Karadağ Öncel E, Öncel MY, Özcay F. A Turkish case of congenital chloride diarrhea with SLC26A3 gene (c.2025_2026insATC) mutation: Diagnostic pitfalls. Turk J Gastroenterol 2010; 21: 443-7
  4. Elrefae F, Elhasanein AF, Alghiaty HA. Congenital chloride diarrhea: a review of twelve Arabian children. Clin Exp Gastroenterol 2013; 6: 71-5
  5. Eğritas O, Dalgic B, Wedenoja S. Congenital chloride diarrhea misdiagnosed as bartter syndrome. Turk J Gastroenterol 2011; 22: 321-3
  6. Langer JC, Winthrop A, Burrows RF, Issenman RM, Caco CC. False diagnosis of intestinal obstruction in a fetus with congenital chloride diarrhea. J Pediatr Surg 1991; 26: 1282-4
  7. Höglund P, Auranen M, Socha J, et al. Genetic background of congenital chloride diarrhea in high incidence populations: Finland, Poland and Saudi Arabia and Kuwait. Am J Hum Genet 1998; 63: 760 -8
  8. Nickavar A. Congenital chloride diarrhea: A case report. Iran J Pediatr 2007; 17: 179-82
  9. Kim SH, Kim SH. Congenital chloride diarrhea: Antenatal ultrasonographic findings in siblings. J Ultrasound Med 2001; 20: 1133-6
  10. Vijayaraghavan B, Lalitha R, Ahmed J. Antenatal diagnosis of congenital chloride diarrhea. Ind J Med Ultrasound 1998; 3&4: 17-18
  11. Imada S, Kikuchi A, Horikoshi T, et al. Prenatal diagnosis and management of congenital chloride diarrhea: A case report of 2 siblings. J Clin Ultrasound 2012; 40: 239-42
  12. Lundkvist K, Annerén G, Esscher T, Ewald U, Hardell LI. Surgical implications of congenital chloride diarrhea. Z Kinderchir 1983; 38: 217-9
  13. Arronson I. Secondary chloride losing diarrhea. Observations on stool electrolytes in infants after bowel surgery. Arch Dis Child 1971; 46: 479-82
  14. Hoglund P, Holmberg C, Sherman P, Kere J. Distenct outcomes of chloride diarrhea in two siblings with identical genetic background of the disease: implications for early diagnosis and treatment. Gut 2001; 48: 724-7.