Unilateral multicystic dysplastic kidney complicated with urinary tract infection by E. coli in a premature newborn
Autosomal recessive polycystic kidney disease is a renal development anomaly characterized by cystic transformation in renal parenchyma. ARPKD is more common in children. We present the case of a premature newborn, female, 36-37 weeks gestation, small for gestational age (SGA) originating from a co...
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| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
Amaltea Medical Publishing House
2024-06-01
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| Series: | Romanian Journal of Pediatrics |
| Subjects: | |
| Online Access: | https://rjp.com.ro/articles/2024.2/RJP_2024_2_Art-11.pdf |
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