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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

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Published in Journal of Medical Case Reports. 2019, vol. 13, no. 1, p. 366
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/embryologyDeliveryObstetricDystocia/diagnostic imagingFemaleFetal Diseases/diagnostic imaging/surgeryFetusGestational AgeHead/diagnostic imaging/embryologyHumansInfantNewbornInterdisciplinary CommunicationMaleNephrectomy/methodsPeritoneal DialysisPolycystic KidneyAutosomal Recessive/diagnostic imaging/embryology/surgeryPregnancyTreatment OutcomeUltrasonographyPrenatalYoung Adult
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PMID: 31829256
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Research group Martinez De Tejada Begona (272)
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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 https://archive-ouverte.unige.ch/unige:139874

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Deposited on : 2020-08-19

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