 |
JOURNAL TOOLS |
| Opzioni di pubblicazione |
| eTOC |
| Per abbonarsi |
| Sottometti un articolo |
| Segnala alla tua biblioteca |
ARTICLE TOOLS |
| Publication history |
| Estratti |
| Permessi |
| Per citare questo articolo |
| Share |
I TUOI DATI
I TUOI ORDINI
CESTINO ACQUISTI
N. prodotti: 0
Totale ordine: € 0,00
COME ORDINARE
I TUOI ABBONAMENTI
I TUOI ARTICOLI
I TUOI EBOOK
COUPON
ACCESSIBILITÀ
CASE REPORT
Gazzetta Medica Italiana - Archivio per le Scienze Mediche 2020 May;179(5):372-4
DOI: 10.23736/S0393-3660.19.04205-0
Copyright © 2019 EDIZIONI MINERVA MEDICA
lingua: Inglese
A fatal case of classic Potter’s Syndrome
Stoyan KOSTOV 1, Angel YORDANOV 2 ✉, Stanislav SLAVCHEV 1, Strahil STRASHILOV 3
1 Clinic of Gynecology, St. Anna University Hospital, Varna, Bulgaria; 2 Department of Gynecologic Oncology, Medical University, Pleven, Bulgaria; 3 Department of Plastic Restorative, Reconstructive and Aesthetic Surgery, Medical University, Pleven, Bulgaria
Potter’s sequence is a rare and fatal disease. There are four types of Potter’s Syndrome. Neonates with classical Potter’s sequence are with oligohydramnios and bilateral renal agenesis. They die shortly after birth because of severe respiratory distress due to pulmonary hypoplasia. Babies have typical physical features - Potter’s face, absence of kidneys and skeletal malformations. We report a fatal case of Potter’s sequence with a typical physical appearance. We performed an autopsy after the delivery.
KEY WORDS: Hereditary renal agenesis; Oligohydramnios; Body physical appearance