EC Paediatrics

Case Report Volume 13 Issue 6 - 2024

Antenatal Diagnosis of Cystic Renal Dysplasia: A Case Report

Zenjali Sara*, Dehayni Fariss, Ankri Majda, Belkouchi Lina, Allali Nazik, Chat Latifa and El Haddad Siham

Department of Pediatric Radiology, Hospital Ibn Sina, Faculty of Medicine and Pharmacy of Rabat, Mohammed V University, Rabat, Morocco

*Corresponding Author: Zenjali Sara, Department of Pediatric Radiology, Hospital Ibn Sina, Faculty of Medicine and Pharmacy of Rabat, Mohammed V University, Rabat, Morocco.
Received: May 08, 2024; Published: May 21, 2024



Multicystic dysplastic kidney (MCDK) is a prevalent renal condition in children, marked by numerous cysts within the kidney that do not communicate with each other and contain minimal to no functional renal tissue. Prenatal diagnosis relies on ultrasound and MRI. Abnormalities detected prenatally, especially those affecting the contralateral kidney, are associated with adverse neonatal outcomes, emphasizing the importance of accurate prenatal assessment for prognosis determination. We present the case of a 42-year-old patient in whom the prenatal diagnosis of unilateral cystic renal dysplasia was made based on antenatal ultrasound and fetal MRI.

 Keywords: Multicystic; Kidney; Dysplastic; Antenatal; MRI; Ultrasound

Zenjali Sara., et al. "Antenatal Diagnosis of Cystic Renal Dysplasia: A Case Report". EC Paediatrics 13.6 (2024): 01-06.