Síndrome de Berdon: diagnóstico intrauterino y evolución posnatal

Teresa Lozoya Araque; José María Vila-Vives; Alfredo Perales-Puchalt; Inmaculada Soler Ferrero; Ramiro Quiroga; Roberto Llorens-Salvador; Antonio Abad Carrascosa; Alfredo Perales

doi:10.1016/j.diapre.2012.08.001

Síndrome de Berdon: diagnóstico intrauterino y evolución posnatal

Translated title of the contribution: Berdon syndrome: Intrauterine diagnosis and postnatal outcome

Teresa Lozoya Araque, José María Vila-Vives, Alfredo Perales-Puchalt, Inmaculada Soler Ferrero, Ramiro Quiroga, Roberto Llorens-Salvador, Antonio Abad Carrascosa, Alfredo Perales

Surgical Oncology

Research output: Contribution to journal › Article › peer-review

3 Scopus citations

Abstract

Berdon syndrome is a rare congenital syndrome characterized by megacystis, microcolon and intestinal hypoperistalsis. It has an ominous prognosis in most cases, and its management requires a multidisciplinary approach. We review a series of cases diagnosed in our center between 1997 and 2010, and discuss the diagnosis, management and outcomes of these patients.

Translated title of the contribution	Berdon syndrome: Intrauterine diagnosis and postnatal outcome
Original language	Spanish
Pages (from-to)	23-28
Number of pages	6
Journal	Diagnostico Prenatal
Volume	24
Issue number	1
DOIs	https://doi.org/10.1016/j.diapre.2012.08.001
State	Published - Jan 2013

Keywords

Berdon syndrome
Intestinal hypoperistalsis
Megacystis
Microcolon

ASJC Scopus subject areas

Obstetrics and Gynecology

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10.1016/j.diapre.2012.08.001

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title = "S{\'i}ndrome de Berdon: diagn{\'o}stico intrauterino y evoluci{\'o}n posnatal",

abstract = "Berdon syndrome is a rare congenital syndrome characterized by megacystis, microcolon and intestinal hypoperistalsis. It has an ominous prognosis in most cases, and its management requires a multidisciplinary approach. We review a series of cases diagnosed in our center between 1997 and 2010, and discuss the diagnosis, management and outcomes of these patients.",

keywords = "Berdon syndrome, Intestinal hypoperistalsis, Megacystis, Microcolon",

author = "{Lozoya Araque}, Teresa and Vila-Vives, {Jos{\'e} Mar{\'i}a} and Alfredo Perales-Puchalt and {Soler Ferrero}, Inmaculada and Ramiro Quiroga and Roberto Llorens-Salvador and {Abad Carrascosa}, Antonio and Alfredo Perales",

year = "2013",

month = jan,

doi = "10.1016/j.diapre.2012.08.001",

language = "Spanish",

volume = "24",

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journal = "Diagnostico Prenatal",

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T1 - Síndrome de Berdon

T2 - diagnóstico intrauterino y evolución posnatal

AU - Lozoya Araque, Teresa

AU - Vila-Vives, José María

AU - Perales-Puchalt, Alfredo

AU - Soler Ferrero, Inmaculada

AU - Quiroga, Ramiro

AU - Llorens-Salvador, Roberto

AU - Abad Carrascosa, Antonio

AU - Perales, Alfredo

PY - 2013/1

Y1 - 2013/1

N2 - Berdon syndrome is a rare congenital syndrome characterized by megacystis, microcolon and intestinal hypoperistalsis. It has an ominous prognosis in most cases, and its management requires a multidisciplinary approach. We review a series of cases diagnosed in our center between 1997 and 2010, and discuss the diagnosis, management and outcomes of these patients.

AB - Berdon syndrome is a rare congenital syndrome characterized by megacystis, microcolon and intestinal hypoperistalsis. It has an ominous prognosis in most cases, and its management requires a multidisciplinary approach. We review a series of cases diagnosed in our center between 1997 and 2010, and discuss the diagnosis, management and outcomes of these patients.

KW - Berdon syndrome

KW - Intestinal hypoperistalsis

KW - Megacystis

KW - Microcolon

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SP - 23

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JO - Diagnostico Prenatal

JF - Diagnostico Prenatal

IS - 1

ER -

Síndrome de Berdon: diagnóstico intrauterino y evolución posnatal

Abstract

Keywords

ASJC Scopus subject areas

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