Journals / Journal of Experimental and Clinical Medicine / 2017 / Volume: 34 Issue: 4

Polyhydramnios and pregnancy complicated with Bartter’s syndrome: A case report

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Publication Date
2019-10-10
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AI Summary & Key Takeaways

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

The infant was healthy at birth and now, is at 4 years of age under constant follow-up by pediatricians.

📌 3 Key Takeaways

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Objective & Hypothesis:0 0 1 122 696 OMU Medical Faculty 5 1 817 14.0 Normal 0 false false false TR JA X-NONE /* Style Definitions */ table.MsoNormalTable {mso-style-name:"Table Normal"; mso-tstyle-rowband-size:0; mso-tstyle-colband-size:0; mso-style-noshow:yes; mso-style-priority:99; mso-style-parent:""; mso-padding-alt:0cm 5.4pt 0cm 5.4pt; mso-para-margin-top:0cm; mso-para-margin-right:0cm; mso-para-margin-bottom:10.0pt; mso-para-margin-left:0cm; line-height:115%; mso-pagination:widow-orphan; font-size:11.0pt; font-family:Calibri; mso-ascii-font-family:Calibri; mso-ascii-theme-font:minor-latin; mso-hansi-font-family:Calibri; mso-hansi-theme-font:minor-latin; mso-ansi-language:TR;} Bartter syndrome is a renal tubular defect that can be diagnosed prenatally, reports are limited on the prenatal course of pregnancies complicated with the disease in the current literature.
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Key Findings & Data:A series of amniocentesis’ were performed until 34 weeks.
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Conclusion & Impact:The infant was healthy at birth and now, is at 4 years of age under constant follow-up by pediatricians.
🔬Design:Review & Systematic Survey
📍Scope:Comprehensive Sample
⚙️Variables:Bartter’s syndrome · Pregnancy · Polyhydramnios

Abstract

0 0 1 122 696 OMU Medical Faculty 5 1 817 14.0 Normal 0 false false false TR JA X-NONE /* Style Definitions */ table.MsoNormalTable {mso-style-name:"Table Normal"; mso-tstyle-rowband-size:0; mso-tstyle-colband-size:0; mso-style-noshow:yes; mso-style-priority:99; mso-style-parent:""; mso-padding-alt:0cm 5.4pt 0cm 5.4pt; mso-para-margin-top:0cm; mso-para-margin-right:0cm; mso-para-margin-bottom:10.0pt; mso-para-margin-left:0cm; line-height:115%; mso-pagination:widow-orphan; font-size:11.0pt; font-family:Calibri; mso-ascii-font-family:Calibri; mso-ascii-theme-font:minor-latin; mso-hansi-font-family:Calibri; mso-hansi-theme-font:minor-latin; mso-ansi-language:TR;} Bartter syndrome is a renal tubular defect that can be diagnosed prenatally, reports are limited on the prenatal course of pregnancies complicated with the disease in the current literature. In this case review we would like to define and debate on the course of pregnancy complicated with Bartter’s syndrome in regard with current literature. Rising levels of polyhydramnios without certain fetal or placental abnormalities should lead us to suspect renal functional disorders like this in which the e valuation of amniotic fluid chloride level is usually diagnostic. A series of amniocentesis’ were performed until 34 weeks. Neonatal and subsequent investigations confirmed the diagnosis of Bartter syndrome. The infant was healthy at birth and now, is at 4 years of age under constant follow-up by pediatricians.

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Cite This Article

Ulubaşoğlu, H., Bakay, K., Güven, D., Koçak, İ. (2019). Polyhydramnios and pregnancy complicated with Bartter’s syndrome: A case report. Journal of Experimental and Clinical Medicine, Volume: 34 Issue: 4. https://ajindex.com/articles/1423409

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References (8)

  1. Amiralok, I., Dawson, K.P., 2000. Bartter syndrome: an overview. Q. J. Med. 93, 207–215.
  2. Bhat, Y., Vinayaka, G., Vani, R., 2011. Antenatal Bartter syndrome: a rare cause of unexplained severe polyhydramnios. Ann. Trop. Paediatr. 31, 153-157.
  3. Moise, K.J., Huhta, J.C., Sharif, D.S., Ou, C.N., Kirshon, B., Wasserstrum, N., Cano L., 1998. Indomethacin in the treatment of premature labor. Effects on the fetal ductus arteriosus. N. Engl. J. Med. 319, 327-331.
  4. Nakanishi, T., Suzumori, N., Mizuno, H., Suzuki, K., Tanemura, T. M., Suzuki, Y., Suzumori, K., 2006. Elevated Aldosterone in Amniotic Fluid and Maternal Blood Has Diagnostic Potential in Pregnancies Complicated with a Fetus of Bartter Syndrome. Fetal Diagn. Ther. 20, 481–484.
  5. Rodrigues, P.R., Hasaart, T., 1982. Hydroamnios and observation in Bartter’s syndrome. Acta Obstet. Gynecol. Scand. 61, 477-478.
  6. Rodriguez-Soriano, J., 2004. Tubular disorders of electrolyte regulation. In: Avner, E., Harmon, W., Niaudet, P., eds. Pediatric Nephrology, 5th edn. Baltimore, MA: Lippincott Williams & Wilkins, pp 729–756.
  7. Smith, L.G., Kirshon, B., Cotton, D.B., 1990. Indomethacin treatment for polyhydramnios and subsequent infantile nephrogenic diabetes insipidus. Am. J. Obstet. Gynecol. 163, 98–99.
  8. Tomoyoshi, N., Toshihide, N.,2001. Pregnancy complicated with Bartter's syndrome. J. Obstet. Gynaecol. 5, 267-274.