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Gyokova, E., Hristova-Atanasova, E., Odumosu, E. and Andreeva, A. (2025) Prenatal Diagnosis of Autosomal Dominant Polycystic Kidney Disease: Case Report. Reports, 8, Article No. 56.
https://doi.org/10.3390/reports8020056

has been cited by the following article:

• TITLE: Renal Polycystic Disease during Pregnancy: A Case Report at the Departmental University Hospital Center of Ouémé, Benin

  AUTHORS: Ingrid Olowo, Moufalilou Aboubakar, Patrice Dangbèmey, Mathieu Ogoudjobi, Tchimon Yéa Sètchégnon Vodounhè, Christiane Tshabu Aguèmon, Josiane Angélique Tonato Bagnan

  KEYWORDS: Autosomal Dominant Polycystic Kidney Disease, Pregnancy, Pseudo-Meigs Syndrome, Renal Failure, Cesarean Section

  JOURNAL NAME: Open Journal of Obstetrics and Gynecology, Vol.16 No.2, February 24, 2026

  ABSTRACT: Renal polycystic disease is a genetic condition that may be revealed or complicated during pregnancy. We report the case of a 24-year-old primigravida admitted to the Departmental University Hospital Center of Ouémé for progressive dyspnea in the context of pregnancy at 35 weeks of amenorrhea, associated with a large abdominal mass, ascites, and pleural effusion. Clinical and paraclinical investigations initially suggested Demons-Meigs syndrome secondary to an ovarian cyst. Cesarean section associated with surgical exploration allowed the diagnosis of renal polycystic disease to be established. This case highlights the diagnostic and therapeutic challenges of renal polycystic disease during pregnancy, as well as its maternal and fetal implications.