http://www.cnr.it/ontology/cnr/individuo/prodotto/ID315496
Prenatal diagnosis and epidemiology of multicystic kidney dysplasia in Europe (Articolo in rivista)
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- Prenatal diagnosis and epidemiology of multicystic kidney dysplasia in Europe (Articolo in rivista) (literal)
- Anno
- 2014-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1002/pd.4433 (literal)
- Alternative label
Winding, Louise; Loane, Maria; Wellesley, Diana; Addor, Marie-Claude; Arriola, Larraitz; Bakker, Marian K.; Bianchi, Fabrizio; Calzolari, Elisa; Gatt, Miriam; Haeusler, Martin; Lelong, Nathalie; Mullaney, Carmel; Scarano, Gioacchino; Tucker, David; Wiesel, Awi; Garne, Ester (2014)
Prenatal diagnosis and epidemiology of multicystic kidney dysplasia in Europe
in Prenatal diagnosis (Print); JOHN WILEY & SONS INC, 605 THIRD AVE, NEW YORK, NY 10158-0012, New York (Stati Uniti d'America)
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- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Winding, Louise; Loane, Maria; Wellesley, Diana; Addor, Marie-Claude; Arriola, Larraitz; Bakker, Marian K.; Bianchi, Fabrizio; Calzolari, Elisa; Gatt, Miriam; Haeusler, Martin; Lelong, Nathalie; Mullaney, Carmel; Scarano, Gioacchino; Tucker, David; Wiesel, Awi; Garne, Ester (literal)
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- http://onlinelibrary.wiley.com/doi/10.1002/pd.4433/pdf (literal)
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- Hosp Lillebaelt; University of Ulster; Princess Anne Hosp; University of Lausanne; University of Barcelona; University of Groningen; CNR Inst Clin Physiol; G Monasterio Tuscany Fdn; University Ferrara Hospital; Directorate Hlth Informat & Res; Medical University of Graz; Centre National de la Recherche Scientifique (CNRS); HSE South South Eas; Regione Campania; PUBL Hlth; Johannes Gutenberg University of Mainz (literal)
- Titolo
- Prenatal diagnosis and epidemiology of multicystic kidney dysplasia in Europe (literal)
- Abstract
- OBJECTIVES:The aim of this study is to describe the prenatal diagnosis and epidemiology of multicystic kidney dysplasia (MCKD).
METHODS:The study is based on routinely collected data from a European database of major congenital anomalies including 13 registries with cases born in 1997-2006 and covering 1 458 552 births.
RESULTS:There were 601 MCKD cases giving an overall prevalence of 4.12 per 10 000 births with regional variation. In live births, 87% of cases had an isolated renal anomaly and 13% had associated major nonrenal anomalies (chromosomal, syndrome or other major anomalies). For the cases with isolated renal anomalies, 51/386 (11%) and 7/386 (2%) choose to terminate the pregnancy or resulted in an intrauterine fetal death, respectively. The prenatal detection rate was 88% in both unilateral and bilateral cases. Birth outcome differed with 92% of unilateral MCKD cases being liveborn compared with 33% of bilateral MCKD cases. For unilateral MCKD cases, 84% had an isolated renal anomaly compared with 51% of bilateral MCKD cases (p < 0.001).
CONCLUSIONS:Cases with unilateral MCKD are mainly liveborn, and only 16% have associated major malformations or a syndrome. Cases with bilateral MCKD are often associated with nonrenal major congenital anomalies or part of a syndrome, and only one third of bilateral MCKD cases in this study were liveborn. Prenatal detection rate of MCKD was high for both unilateral and bilateral cases. © 2014 John Wiley & Sons, Ltd. (literal)
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