Síndrome de Currarino y enfermedad de Hirschsprung: Una asociación poco frecuente Currarino´s syndrome and Hirschsprung´s disease: A rare combination

El Síndrome de Currarino consiste en agenesia sacra parcial de herencia genética autosómica dominante parcial, que afecta las vértebras sacras S2 a S5, preservándose S1. En la forma más severa del síndrome, a la agenesia sacra se asocian masa presacra y malformaciones anorrectales y urogenitales. La...
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Autor*in:	David Ibáñez M [verfasserIn] Ana Vela M [verfasserIn] Beatriz Izquierdo H [verfasserIn] Carolina Muel G [verfasserIn]

Format:	E-Artikel
Sprache:	Spanisch

Erschienen:	2012

Schlagwörter:	Atresia rectal Masa presacra Enfermedad de Hirschsprung Síndrome de Currarino Currarino syndrome Hirschsprung´s disease Presacral mass Rectal atresia

Übergeordnetes Werk:	In: Revista Chilena de Radiología - Permanyer, 2022, 18(2012), 4, Seite 175-178
Übergeordnetes Werk:	volume:18 ; year:2012 ; number:4 ; pages:175-178

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Katalog-ID:	DOAJ047998601

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520			\|a El Síndrome de Currarino consiste en agenesia sacra parcial de herencia genética autosómica dominante parcial, que afecta las vértebras sacras S2 a S5, preservándose S1. En la forma más severa del síndrome, a la agenesia sacra se asocian masa presacra y malformaciones anorrectales y urogenitales. La enfermedad de Hirschsprung es una malformación congénita del intestino grueso debida a la ausencia de células ganglionares intrínsecas parasimpáticas de la submucosa y de los plexos mientéricos. Presentamos el caso de un niño de 3 años con Síndrome de Currarino asociado a enfermedad de Hirschsprung.<br<The Currarino syndrome is an autosomal dominant partial sacral agenesis involving sacral vertebrae S2 to S5, with presevation of the S1 vertebrae. In the most severe form of the syndrome, the sacral agenesis is associated to presacral mass, anorrectal and urogenital malformations. Hirschsprung´s disease is a congenital malformation of the hindgut determined by the absence if parasympathetic intrinsic ganglion cells in the submucosal and myenteric plexuses. We present a case of a 3 years old male child affected from Currarino syndrome associated to Hirschprung´s disease.
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650		4	\|a Presacral mass
650		4	\|a Rectal atresia
653		0	\|a Medical physics. Medical radiology. Nuclear medicine
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allfields	(DE-627)DOAJ047998601 (DE-599)DOAJ85e78a8b1f6d44a6937975a220956a25 DE-627 ger DE-627 rakwb spa R895-920 R855-855.5 David Ibáñez M verfasserin aut Síndrome de Currarino y enfermedad de Hirschsprung: Una asociación poco frecuente Currarino´s syndrome and Hirschsprung´s disease: A rare combination 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier El Síndrome de Currarino consiste en agenesia sacra parcial de herencia genética autosómica dominante parcial, que afecta las vértebras sacras S2 a S5, preservándose S1. En la forma más severa del síndrome, a la agenesia sacra se asocian masa presacra y malformaciones anorrectales y urogenitales. La enfermedad de Hirschsprung es una malformación congénita del intestino grueso debida a la ausencia de células ganglionares intrínsecas parasimpáticas de la submucosa y de los plexos mientéricos. Presentamos el caso de un niño de 3 años con Síndrome de Currarino asociado a enfermedad de Hirschsprung.<br<The Currarino syndrome is an autosomal dominant partial sacral agenesis involving sacral vertebrae S2 to S5, with presevation of the S1 vertebrae. In the most severe form of the syndrome, the sacral agenesis is associated to presacral mass, anorrectal and urogenital malformations. Hirschsprung´s disease is a congenital malformation of the hindgut determined by the absence if parasympathetic intrinsic ganglion cells in the submucosal and myenteric plexuses. We present a case of a 3 years old male child affected from Currarino syndrome associated to Hirschprung´s disease. Atresia rectal Masa presacra Enfermedad de Hirschsprung Síndrome de Currarino Currarino syndrome Hirschsprung´s disease Presacral mass Rectal atresia Medical physics. Medical radiology. Nuclear medicine Medical technology Ana Vela M verfasserin aut Beatriz Izquierdo H verfasserin aut Carolina Muel G verfasserin aut In Revista Chilena de Radiología Permanyer, 2022 18(2012), 4, Seite 175-178 (DE-627)363749071 (DE-600)2105109-4 07179308 nnns volume:18 year:2012 number:4 pages:175-178 https://doaj.org/article/85e78a8b1f6d44a6937975a220956a25 kostenfrei http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-93082012000400006 kostenfrei https://doaj.org/toc/0717-201X Journal toc kostenfrei https://doaj.org/toc/0717-9308 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 18 2012 4 175-178
spelling	(DE-627)DOAJ047998601 (DE-599)DOAJ85e78a8b1f6d44a6937975a220956a25 DE-627 ger DE-627 rakwb spa R895-920 R855-855.5 David Ibáñez M verfasserin aut Síndrome de Currarino y enfermedad de Hirschsprung: Una asociación poco frecuente Currarino´s syndrome and Hirschsprung´s disease: A rare combination 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier El Síndrome de Currarino consiste en agenesia sacra parcial de herencia genética autosómica dominante parcial, que afecta las vértebras sacras S2 a S5, preservándose S1. En la forma más severa del síndrome, a la agenesia sacra se asocian masa presacra y malformaciones anorrectales y urogenitales. La enfermedad de Hirschsprung es una malformación congénita del intestino grueso debida a la ausencia de células ganglionares intrínsecas parasimpáticas de la submucosa y de los plexos mientéricos. Presentamos el caso de un niño de 3 años con Síndrome de Currarino asociado a enfermedad de Hirschsprung.<br<The Currarino syndrome is an autosomal dominant partial sacral agenesis involving sacral vertebrae S2 to S5, with presevation of the S1 vertebrae. In the most severe form of the syndrome, the sacral agenesis is associated to presacral mass, anorrectal and urogenital malformations. Hirschsprung´s disease is a congenital malformation of the hindgut determined by the absence if parasympathetic intrinsic ganglion cells in the submucosal and myenteric plexuses. We present a case of a 3 years old male child affected from Currarino syndrome associated to Hirschprung´s disease. Atresia rectal Masa presacra Enfermedad de Hirschsprung Síndrome de Currarino Currarino syndrome Hirschsprung´s disease Presacral mass Rectal atresia Medical physics. Medical radiology. Nuclear medicine Medical technology Ana Vela M verfasserin aut Beatriz Izquierdo H verfasserin aut Carolina Muel G verfasserin aut In Revista Chilena de Radiología Permanyer, 2022 18(2012), 4, Seite 175-178 (DE-627)363749071 (DE-600)2105109-4 07179308 nnns volume:18 year:2012 number:4 pages:175-178 https://doaj.org/article/85e78a8b1f6d44a6937975a220956a25 kostenfrei http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-93082012000400006 kostenfrei https://doaj.org/toc/0717-201X Journal toc kostenfrei https://doaj.org/toc/0717-9308 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 18 2012 4 175-178
allfields_unstemmed	(DE-627)DOAJ047998601 (DE-599)DOAJ85e78a8b1f6d44a6937975a220956a25 DE-627 ger DE-627 rakwb spa R895-920 R855-855.5 David Ibáñez M verfasserin aut Síndrome de Currarino y enfermedad de Hirschsprung: Una asociación poco frecuente Currarino´s syndrome and Hirschsprung´s disease: A rare combination 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier El Síndrome de Currarino consiste en agenesia sacra parcial de herencia genética autosómica dominante parcial, que afecta las vértebras sacras S2 a S5, preservándose S1. En la forma más severa del síndrome, a la agenesia sacra se asocian masa presacra y malformaciones anorrectales y urogenitales. La enfermedad de Hirschsprung es una malformación congénita del intestino grueso debida a la ausencia de células ganglionares intrínsecas parasimpáticas de la submucosa y de los plexos mientéricos. Presentamos el caso de un niño de 3 años con Síndrome de Currarino asociado a enfermedad de Hirschsprung.<br<The Currarino syndrome is an autosomal dominant partial sacral agenesis involving sacral vertebrae S2 to S5, with presevation of the S1 vertebrae. In the most severe form of the syndrome, the sacral agenesis is associated to presacral mass, anorrectal and urogenital malformations. Hirschsprung´s disease is a congenital malformation of the hindgut determined by the absence if parasympathetic intrinsic ganglion cells in the submucosal and myenteric plexuses. We present a case of a 3 years old male child affected from Currarino syndrome associated to Hirschprung´s disease. Atresia rectal Masa presacra Enfermedad de Hirschsprung Síndrome de Currarino Currarino syndrome Hirschsprung´s disease Presacral mass Rectal atresia Medical physics. Medical radiology. Nuclear medicine Medical technology Ana Vela M verfasserin aut Beatriz Izquierdo H verfasserin aut Carolina Muel G verfasserin aut In Revista Chilena de Radiología Permanyer, 2022 18(2012), 4, Seite 175-178 (DE-627)363749071 (DE-600)2105109-4 07179308 nnns volume:18 year:2012 number:4 pages:175-178 https://doaj.org/article/85e78a8b1f6d44a6937975a220956a25 kostenfrei http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-93082012000400006 kostenfrei https://doaj.org/toc/0717-201X Journal toc kostenfrei https://doaj.org/toc/0717-9308 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 18 2012 4 175-178
allfieldsGer	(DE-627)DOAJ047998601 (DE-599)DOAJ85e78a8b1f6d44a6937975a220956a25 DE-627 ger DE-627 rakwb spa R895-920 R855-855.5 David Ibáñez M verfasserin aut Síndrome de Currarino y enfermedad de Hirschsprung: Una asociación poco frecuente Currarino´s syndrome and Hirschsprung´s disease: A rare combination 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier El Síndrome de Currarino consiste en agenesia sacra parcial de herencia genética autosómica dominante parcial, que afecta las vértebras sacras S2 a S5, preservándose S1. En la forma más severa del síndrome, a la agenesia sacra se asocian masa presacra y malformaciones anorrectales y urogenitales. La enfermedad de Hirschsprung es una malformación congénita del intestino grueso debida a la ausencia de células ganglionares intrínsecas parasimpáticas de la submucosa y de los plexos mientéricos. Presentamos el caso de un niño de 3 años con Síndrome de Currarino asociado a enfermedad de Hirschsprung.<br<The Currarino syndrome is an autosomal dominant partial sacral agenesis involving sacral vertebrae S2 to S5, with presevation of the S1 vertebrae. In the most severe form of the syndrome, the sacral agenesis is associated to presacral mass, anorrectal and urogenital malformations. Hirschsprung´s disease is a congenital malformation of the hindgut determined by the absence if parasympathetic intrinsic ganglion cells in the submucosal and myenteric plexuses. We present a case of a 3 years old male child affected from Currarino syndrome associated to Hirschprung´s disease. Atresia rectal Masa presacra Enfermedad de Hirschsprung Síndrome de Currarino Currarino syndrome Hirschsprung´s disease Presacral mass Rectal atresia Medical physics. Medical radiology. Nuclear medicine Medical technology Ana Vela M verfasserin aut Beatriz Izquierdo H verfasserin aut Carolina Muel G verfasserin aut In Revista Chilena de Radiología Permanyer, 2022 18(2012), 4, Seite 175-178 (DE-627)363749071 (DE-600)2105109-4 07179308 nnns volume:18 year:2012 number:4 pages:175-178 https://doaj.org/article/85e78a8b1f6d44a6937975a220956a25 kostenfrei http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-93082012000400006 kostenfrei https://doaj.org/toc/0717-201X Journal toc kostenfrei https://doaj.org/toc/0717-9308 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 18 2012 4 175-178
allfieldsSound	(DE-627)DOAJ047998601 (DE-599)DOAJ85e78a8b1f6d44a6937975a220956a25 DE-627 ger DE-627 rakwb spa R895-920 R855-855.5 David Ibáñez M verfasserin aut Síndrome de Currarino y enfermedad de Hirschsprung: Una asociación poco frecuente Currarino´s syndrome and Hirschsprung´s disease: A rare combination 2012 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier El Síndrome de Currarino consiste en agenesia sacra parcial de herencia genética autosómica dominante parcial, que afecta las vértebras sacras S2 a S5, preservándose S1. En la forma más severa del síndrome, a la agenesia sacra se asocian masa presacra y malformaciones anorrectales y urogenitales. La enfermedad de Hirschsprung es una malformación congénita del intestino grueso debida a la ausencia de células ganglionares intrínsecas parasimpáticas de la submucosa y de los plexos mientéricos. Presentamos el caso de un niño de 3 años con Síndrome de Currarino asociado a enfermedad de Hirschsprung.<br<The Currarino syndrome is an autosomal dominant partial sacral agenesis involving sacral vertebrae S2 to S5, with presevation of the S1 vertebrae. In the most severe form of the syndrome, the sacral agenesis is associated to presacral mass, anorrectal and urogenital malformations. Hirschsprung´s disease is a congenital malformation of the hindgut determined by the absence if parasympathetic intrinsic ganglion cells in the submucosal and myenteric plexuses. We present a case of a 3 years old male child affected from Currarino syndrome associated to Hirschprung´s disease. Atresia rectal Masa presacra Enfermedad de Hirschsprung Síndrome de Currarino Currarino syndrome Hirschsprung´s disease Presacral mass Rectal atresia Medical physics. Medical radiology. Nuclear medicine Medical technology Ana Vela M verfasserin aut Beatriz Izquierdo H verfasserin aut Carolina Muel G verfasserin aut In Revista Chilena de Radiología Permanyer, 2022 18(2012), 4, Seite 175-178 (DE-627)363749071 (DE-600)2105109-4 07179308 nnns volume:18 year:2012 number:4 pages:175-178 https://doaj.org/article/85e78a8b1f6d44a6937975a220956a25 kostenfrei http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-93082012000400006 kostenfrei https://doaj.org/toc/0717-201X Journal toc kostenfrei https://doaj.org/toc/0717-9308 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 18 2012 4 175-178
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En la forma más severa del síndrome, a la agenesia sacra se asocian masa presacra y malformaciones anorrectales y urogenitales. La enfermedad de Hirschsprung es una malformación congénita del intestino grueso debida a la ausencia de células ganglionares intrínsecas parasimpáticas de la submucosa y de los plexos mientéricos. Presentamos el caso de un niño de 3 años con Síndrome de Currarino asociado a enfermedad de Hirschsprung.<br<The Currarino syndrome is an autosomal dominant partial sacral agenesis involving sacral vertebrae S2 to S5, with presevation of the S1 vertebrae. In the most severe form of the syndrome, the sacral agenesis is associated to presacral mass, anorrectal and urogenital malformations. Hirschsprung´s disease is a congenital malformation of the hindgut determined by the absence if parasympathetic intrinsic ganglion cells in the submucosal and myenteric plexuses. 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callnumber-first	R - Medicine
author	David Ibáñez M
spellingShingle	David Ibáñez M misc R895-920 misc R855-855.5 misc Atresia rectal misc Masa presacra misc Enfermedad de Hirschsprung misc Síndrome de Currarino misc Currarino syndrome misc Hirschsprung´s disease misc Presacral mass misc Rectal atresia misc Medical physics. Medical radiology. Nuclear medicine misc Medical technology Síndrome de Currarino y enfermedad de Hirschsprung: Una asociación poco frecuente Currarino´s syndrome and Hirschsprung´s disease: A rare combination
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topic_title	R895-920 R855-855.5 Síndrome de Currarino y enfermedad de Hirschsprung: Una asociación poco frecuente Currarino´s syndrome and Hirschsprung´s disease: A rare combination Atresia rectal Masa presacra Enfermedad de Hirschsprung Síndrome de Currarino Currarino syndrome Hirschsprung´s disease Presacral mass Rectal atresia
topic	misc R895-920 misc R855-855.5 misc Atresia rectal misc Masa presacra misc Enfermedad de Hirschsprung misc Síndrome de Currarino misc Currarino syndrome misc Hirschsprung´s disease misc Presacral mass misc Rectal atresia misc Medical physics. Medical radiology. Nuclear medicine misc Medical technology
topic_unstemmed	misc R895-920 misc R855-855.5 misc Atresia rectal misc Masa presacra misc Enfermedad de Hirschsprung misc Síndrome de Currarino misc Currarino syndrome misc Hirschsprung´s disease misc Presacral mass misc Rectal atresia misc Medical physics. Medical radiology. Nuclear medicine misc Medical technology
topic_browse	misc R895-920 misc R855-855.5 misc Atresia rectal misc Masa presacra misc Enfermedad de Hirschsprung misc Síndrome de Currarino misc Currarino syndrome misc Hirschsprung´s disease misc Presacral mass misc Rectal atresia misc Medical physics. Medical radiology. Nuclear medicine misc Medical technology
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title	Síndrome de Currarino y enfermedad de Hirschsprung: Una asociación poco frecuente Currarino´s syndrome and Hirschsprung´s disease: A rare combination
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title_full	Síndrome de Currarino y enfermedad de Hirschsprung: Una asociación poco frecuente Currarino´s syndrome and Hirschsprung´s disease: A rare combination
author_sort	David Ibáñez M
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author_browse	David Ibáñez M Ana Vela M Beatriz Izquierdo H Carolina Muel G
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title_sort	síndrome de currarino y enfermedad de hirschsprung: una asociación poco frecuente currarino´s syndrome and hirschsprung´s disease: a rare combination
callnumber	R895-920
title_auth	Síndrome de Currarino y enfermedad de Hirschsprung: Una asociación poco frecuente Currarino´s syndrome and Hirschsprung´s disease: A rare combination
abstract	El Síndrome de Currarino consiste en agenesia sacra parcial de herencia genética autosómica dominante parcial, que afecta las vértebras sacras S2 a S5, preservándose S1. En la forma más severa del síndrome, a la agenesia sacra se asocian masa presacra y malformaciones anorrectales y urogenitales. La enfermedad de Hirschsprung es una malformación congénita del intestino grueso debida a la ausencia de células ganglionares intrínsecas parasimpáticas de la submucosa y de los plexos mientéricos. Presentamos el caso de un niño de 3 años con Síndrome de Currarino asociado a enfermedad de Hirschsprung.<br<The Currarino syndrome is an autosomal dominant partial sacral agenesis involving sacral vertebrae S2 to S5, with presevation of the S1 vertebrae. In the most severe form of the syndrome, the sacral agenesis is associated to presacral mass, anorrectal and urogenital malformations. Hirschsprung´s disease is a congenital malformation of the hindgut determined by the absence if parasympathetic intrinsic ganglion cells in the submucosal and myenteric plexuses. We present a case of a 3 years old male child affected from Currarino syndrome associated to Hirschprung´s disease.
abstractGer	El Síndrome de Currarino consiste en agenesia sacra parcial de herencia genética autosómica dominante parcial, que afecta las vértebras sacras S2 a S5, preservándose S1. En la forma más severa del síndrome, a la agenesia sacra se asocian masa presacra y malformaciones anorrectales y urogenitales. La enfermedad de Hirschsprung es una malformación congénita del intestino grueso debida a la ausencia de células ganglionares intrínsecas parasimpáticas de la submucosa y de los plexos mientéricos. Presentamos el caso de un niño de 3 años con Síndrome de Currarino asociado a enfermedad de Hirschsprung.<br<The Currarino syndrome is an autosomal dominant partial sacral agenesis involving sacral vertebrae S2 to S5, with presevation of the S1 vertebrae. In the most severe form of the syndrome, the sacral agenesis is associated to presacral mass, anorrectal and urogenital malformations. Hirschsprung´s disease is a congenital malformation of the hindgut determined by the absence if parasympathetic intrinsic ganglion cells in the submucosal and myenteric plexuses. We present a case of a 3 years old male child affected from Currarino syndrome associated to Hirschprung´s disease.
abstract_unstemmed	El Síndrome de Currarino consiste en agenesia sacra parcial de herencia genética autosómica dominante parcial, que afecta las vértebras sacras S2 a S5, preservándose S1. En la forma más severa del síndrome, a la agenesia sacra se asocian masa presacra y malformaciones anorrectales y urogenitales. La enfermedad de Hirschsprung es una malformación congénita del intestino grueso debida a la ausencia de células ganglionares intrínsecas parasimpáticas de la submucosa y de los plexos mientéricos. Presentamos el caso de un niño de 3 años con Síndrome de Currarino asociado a enfermedad de Hirschsprung.<br<The Currarino syndrome is an autosomal dominant partial sacral agenesis involving sacral vertebrae S2 to S5, with presevation of the S1 vertebrae. In the most severe form of the syndrome, the sacral agenesis is associated to presacral mass, anorrectal and urogenital malformations. Hirschsprung´s disease is a congenital malformation of the hindgut determined by the absence if parasympathetic intrinsic ganglion cells in the submucosal and myenteric plexuses. We present a case of a 3 years old male child affected from Currarino syndrome associated to Hirschprung´s disease.
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title_short	Síndrome de Currarino y enfermedad de Hirschsprung: Una asociación poco frecuente Currarino´s syndrome and Hirschsprung´s disease: A rare combination
url	https://doaj.org/article/85e78a8b1f6d44a6937975a220956a25 http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-93082012000400006 https://doaj.org/toc/0717-201X https://doaj.org/toc/0717-9308
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En la forma más severa del síndrome, a la agenesia sacra se asocian masa presacra y malformaciones anorrectales y urogenitales. La enfermedad de Hirschsprung es una malformación congénita del intestino grueso debida a la ausencia de células ganglionares intrínsecas parasimpáticas de la submucosa y de los plexos mientéricos. Presentamos el caso de un niño de 3 años con Síndrome de Currarino asociado a enfermedad de Hirschsprung.<br<The Currarino syndrome is an autosomal dominant partial sacral agenesis involving sacral vertebrae S2 to S5, with presevation of the S1 vertebrae. In the most severe form of the syndrome, the sacral agenesis is associated to presacral mass, anorrectal and urogenital malformations. Hirschsprung´s disease is a congenital malformation of the hindgut determined by the absence if parasympathetic intrinsic ganglion cells in the submucosal and myenteric plexuses. 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Síndrome de Currarino y enfermedad de Hirschsprung: Una asociación poco frecuente Currarino´s syndrome and Hirschsprung´s disease: A rare combination

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