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Titolo:
Prenatal diagnosis of renal dysplasia
Autore:
Strauss, A; Hasbargen, U; Paek, B; Fuchshuber, S; Hepp, H;
Indirizzi:
Univ Munich, Klinikum Grosshadern, Klin & Poliklin Frauenheilkunde & Geburtshilfe, D-81377 Munich, Germany Univ Munich Munich Germany D-81377 Geburtshilfe, D-81377 Munich, Germany Univ Calif San Francisco, Fetal Treatment Ctr, Dept Surg, Div Pediat Surg,San Francisco, CA 94143 USA Univ Calif San Francisco San Francisco CA USA 94143 ancisco, CA 94143 USA
Titolo Testata:
ZEITSCHRIFT FUR GEBURTSHILFE UND NEONATOLOGIE
fascicolo: 2, volume: 205, anno: 2001,
pagine: 71 - 75
SICI:
0948-2393(200103/04)205:2<71:PDORD>2.0.ZU;2-5
Fonte:
ISI
Lingua:
GER
Keywords:
renal dysplasia; renal agenesis; Potter syndrome; Potter sequence;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Clinical Medicine
Citazioni:
11
Recensione:
Indirizzi per estratti:
Indirizzo: Strauss, A Univ Munich, Klinikum Grosshadern, Klin & Poliklin Frauenheilkunde & Geburtshilfe, Marchioninistr 15, D-81377 Munich, Germany Univ Munich Marchioninistr 15 Munich Germany D-81377 , Germany
Citazione:
A. Strauss et al., "Prenatal diagnosis of renal dysplasia", Z GEBU NEON, 205(2), 2001, pp. 71-75

Abstract

Background: Aside from congenital anomalies of the urogenital tract, fetalrenal tissue itself can be dysplastic. Prenatal ultrasound allows the differential diagnosis of simple cysts, different degrees of renal dysplasia and agenesis of the kidneys. Materials and methods: This article focuses on the multifactorious complexof parenchymal renal disease. According to the classification of Potter Syndrome and cystic renal dysplasia/Potter Sequences I-IV, pathogenesis, prenatal diagnosis, pre- and postnatal treatment options and prognosis are discussed. Results and discussion: Concomitant absence of amniotic fluid frequently refutes diagnosis until artificial amniotic fluid infusion has been performed. Although intrauterine therapy is rarely possible, the frequent association with other abnormalities and fetal syndromes may be of consequence. The sonographic appearance of parenchymal renal disease is heterogeneous, This inconsistency has lead to different classifications. This study uses the "modified Potter Classification" of parenchymal disease in kidneys (Zerres),Bilateral renal agenesis Potter SyndromeInfantile polycystic kidney disease Potter Type IAdult polycystic kidney disease Potter Type IIIMulticystic kidney disease Potter Type IICortical cystic kidney disease Potter Type IVConclusion: Prognosis is variable, ranging from excellent to incurable.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 27/11/20 alle ore 10:10:15