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Management of delivery of a fetus with autosomal recessive polycystic kidney disease: a case report of abdominal dystocia and review of the literature

Published inJournal of Medical Case Reports, vol. 13, no. 1, 366
Publication date2019
Abstract

Autosomal recessive renal polycystic kidney disease occurs in 1 in 20,000 live births. It is caused by mutations in both alleles of the PKHD1 gene. Management of delivery in cases of suspected autosomal recessive renal polycystic kidney disease is rarely discussed, and literature concerning abdominal dystocia is extremely scarce. We present a case of a patient with autosomal recessive renal polycystic kidney disease whose delivery was complicated by abdominal dystocia, and we discuss the factors that determined the route and timing of delivery.

Keywords
  • Abdomen/abnormalities/diagnostic imaging/embryology
  • Delivery
  • Obstetric
  • Dystocia/diagnostic imaging
  • Female
  • Fetal Diseases/diagnostic imaging/surgery
  • Fetus
  • Gestational Age
  • Head/diagnostic imaging/embryology
  • Humans
  • Infant
  • Newborn
  • Interdisciplinary Communication
  • Male
  • Nephrectomy/methods
  • Peritoneal Dialysis
  • Polycystic Kidney
  • Autosomal Recessive/diagnostic imaging/embryology/surgery
  • Pregnancy
  • Treatment Outcome
  • Ultrasonography
  • Prenatal
  • Young Adult
Citation (ISO format)
BELIN, Sarah et al. Management of delivery of a fetus with autosomal recessive polycystic kidney disease: a case report of abdominal dystocia and review of the literature. In: Journal of Medical Case Reports, 2019, vol. 13, n° 1, p. 366. doi: 10.1186/s13256-019-2293-3
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Article (Published version)
Identifiers
Journal ISSN1752-1947
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563downloads

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