Congenital Pyloric Atresia: Experience with a Series of 11 Cases and Collective Review

Introduction: Pyloric atresia is a rare cause of congenital gastric outlet obstruction. It is often associated with epidermolysis bullosa (EB). Rarity and experience with 11 cases are the reason for this publication. Aims and Objectives: The aim and objective of this study is to present our experien...
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Autor*in:	Gungi Raghavendra Prasad [verfasserIn] J V Subba Rao [verfasserIn] Firdous Fatima [verfasserIn] Fariha Anjum [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2021

Schlagwörter:	epidermolysis bullosa polyhydramnios pyloric atresia

Übergeordnetes Werk:	In: Journal of Indian Association of Pediatric Surgeons - Wolters Kluwer Medknow Publications, 2004, 26(2021), 6, Seite 416-420
Übergeordnetes Werk:	volume:26 ; year:2021 ; number:6 ; pages:416-420

Links:	Link aufrufen Link aufrufen Link aufrufen Journal toc Journal toc

DOI / URN:	10.4103/jiaps.JIAPS_295_20

Katalog-ID:	DOAJ067610900

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520			\|a Introduction: Pyloric atresia is a rare cause of congenital gastric outlet obstruction. It is often associated with epidermolysis bullosa (EB). Rarity and experience with 11 cases are the reason for this publication. Aims and Objectives: The aim and objective of this study is to present our experience of 11 cases of congenital pyloric atresia and correlate with available literature. Materials and Methods: This was retrospective cohort of 11 cases correlative comparative study. Data of all the 11 cases from 1982 to 2019 were collected, reviewed, and analyzed. The parameters studied included age, gender, antenatal diagnosis, postnatal diagnosis, preoperative management, intraoperative findings, postoperative course outcome, associated anomalies, and any genetic studies if done. All these parameters were compared with published data. Results: There were 11 cases in the present series with six boys and five girls. Most of them presented at varying periods from birth to day 1 of life. Eight cases of type 1 pyloric atresia, two cases of type 2 pyloric atresia, and one case of type 3 pyloric atresia constituted the cohort. Five out of 11 cases were associated with EB. Two out of six cases with isolated pyloric atresia and four out of five cases with EB died. Discussion: Congenital pyloric atresia may be isolated or associated with EB. Three varieties of pyloric atresia were described. Association with EB increases the mortality. Conclusions: Review and analysis of 11 cases of pyloric atresia compared with published literature is being reported.
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spelling	10.4103/jiaps.JIAPS_295_20 doi (DE-627)DOAJ067610900 (DE-599)DOAJc555429cd392434196f36bbabc7f2fd8 DE-627 ger DE-627 rakwb eng RJ1-570 RD1-811 Gungi Raghavendra Prasad verfasserin aut Congenital Pyloric Atresia: Experience with a Series of 11 Cases and Collective Review 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Introduction: Pyloric atresia is a rare cause of congenital gastric outlet obstruction. It is often associated with epidermolysis bullosa (EB). Rarity and experience with 11 cases are the reason for this publication. Aims and Objectives: The aim and objective of this study is to present our experience of 11 cases of congenital pyloric atresia and correlate with available literature. Materials and Methods: This was retrospective cohort of 11 cases correlative comparative study. Data of all the 11 cases from 1982 to 2019 were collected, reviewed, and analyzed. The parameters studied included age, gender, antenatal diagnosis, postnatal diagnosis, preoperative management, intraoperative findings, postoperative course outcome, associated anomalies, and any genetic studies if done. All these parameters were compared with published data. Results: There were 11 cases in the present series with six boys and five girls. Most of them presented at varying periods from birth to day 1 of life. Eight cases of type 1 pyloric atresia, two cases of type 2 pyloric atresia, and one case of type 3 pyloric atresia constituted the cohort. Five out of 11 cases were associated with EB. Two out of six cases with isolated pyloric atresia and four out of five cases with EB died. Discussion: Congenital pyloric atresia may be isolated or associated with EB. Three varieties of pyloric atresia were described. Association with EB increases the mortality. Conclusions: Review and analysis of 11 cases of pyloric atresia compared with published literature is being reported. epidermolysis bullosa polyhydramnios pyloric atresia Pediatrics Surgery J V Subba Rao verfasserin aut Firdous Fatima verfasserin aut Fariha Anjum verfasserin aut In Journal of Indian Association of Pediatric Surgeons Wolters Kluwer Medknow Publications, 2004 26(2021), 6, Seite 416-420 (DE-627)461908964 (DE-600)2164528-0 19983891 nnns volume:26 year:2021 number:6 pages:416-420 https://doi.org/10.4103/jiaps.JIAPS_295_20 kostenfrei https://doaj.org/article/c555429cd392434196f36bbabc7f2fd8 kostenfrei http://www.jiaps.com/article.asp?issn=0971-9261;year=2021;volume=26;issue=6;spage=416;epage=420;aulast=Prasad kostenfrei https://doaj.org/toc/0971-9261 Journal toc kostenfrei https://doaj.org/toc/1998-3891 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 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_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 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 26 2021 6 416-420
allfields_unstemmed	10.4103/jiaps.JIAPS_295_20 doi (DE-627)DOAJ067610900 (DE-599)DOAJc555429cd392434196f36bbabc7f2fd8 DE-627 ger DE-627 rakwb eng RJ1-570 RD1-811 Gungi Raghavendra Prasad verfasserin aut Congenital Pyloric Atresia: Experience with a Series of 11 Cases and Collective Review 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Introduction: Pyloric atresia is a rare cause of congenital gastric outlet obstruction. It is often associated with epidermolysis bullosa (EB). Rarity and experience with 11 cases are the reason for this publication. Aims and Objectives: The aim and objective of this study is to present our experience of 11 cases of congenital pyloric atresia and correlate with available literature. Materials and Methods: This was retrospective cohort of 11 cases correlative comparative study. Data of all the 11 cases from 1982 to 2019 were collected, reviewed, and analyzed. The parameters studied included age, gender, antenatal diagnosis, postnatal diagnosis, preoperative management, intraoperative findings, postoperative course outcome, associated anomalies, and any genetic studies if done. All these parameters were compared with published data. Results: There were 11 cases in the present series with six boys and five girls. Most of them presented at varying periods from birth to day 1 of life. Eight cases of type 1 pyloric atresia, two cases of type 2 pyloric atresia, and one case of type 3 pyloric atresia constituted the cohort. Five out of 11 cases were associated with EB. Two out of six cases with isolated pyloric atresia and four out of five cases with EB died. Discussion: Congenital pyloric atresia may be isolated or associated with EB. Three varieties of pyloric atresia were described. Association with EB increases the mortality. Conclusions: Review and analysis of 11 cases of pyloric atresia compared with published literature is being reported. epidermolysis bullosa polyhydramnios pyloric atresia Pediatrics Surgery J V Subba Rao verfasserin aut Firdous Fatima verfasserin aut Fariha Anjum verfasserin aut In Journal of Indian Association of Pediatric Surgeons Wolters Kluwer Medknow Publications, 2004 26(2021), 6, Seite 416-420 (DE-627)461908964 (DE-600)2164528-0 19983891 nnns volume:26 year:2021 number:6 pages:416-420 https://doi.org/10.4103/jiaps.JIAPS_295_20 kostenfrei https://doaj.org/article/c555429cd392434196f36bbabc7f2fd8 kostenfrei http://www.jiaps.com/article.asp?issn=0971-9261;year=2021;volume=26;issue=6;spage=416;epage=420;aulast=Prasad kostenfrei https://doaj.org/toc/0971-9261 Journal toc kostenfrei https://doaj.org/toc/1998-3891 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 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_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 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 26 2021 6 416-420
allfieldsGer	10.4103/jiaps.JIAPS_295_20 doi (DE-627)DOAJ067610900 (DE-599)DOAJc555429cd392434196f36bbabc7f2fd8 DE-627 ger DE-627 rakwb eng RJ1-570 RD1-811 Gungi Raghavendra Prasad verfasserin aut Congenital Pyloric Atresia: Experience with a Series of 11 Cases and Collective Review 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Introduction: Pyloric atresia is a rare cause of congenital gastric outlet obstruction. It is often associated with epidermolysis bullosa (EB). Rarity and experience with 11 cases are the reason for this publication. Aims and Objectives: The aim and objective of this study is to present our experience of 11 cases of congenital pyloric atresia and correlate with available literature. Materials and Methods: This was retrospective cohort of 11 cases correlative comparative study. Data of all the 11 cases from 1982 to 2019 were collected, reviewed, and analyzed. The parameters studied included age, gender, antenatal diagnosis, postnatal diagnosis, preoperative management, intraoperative findings, postoperative course outcome, associated anomalies, and any genetic studies if done. All these parameters were compared with published data. Results: There were 11 cases in the present series with six boys and five girls. Most of them presented at varying periods from birth to day 1 of life. Eight cases of type 1 pyloric atresia, two cases of type 2 pyloric atresia, and one case of type 3 pyloric atresia constituted the cohort. Five out of 11 cases were associated with EB. Two out of six cases with isolated pyloric atresia and four out of five cases with EB died. Discussion: Congenital pyloric atresia may be isolated or associated with EB. Three varieties of pyloric atresia were described. Association with EB increases the mortality. Conclusions: Review and analysis of 11 cases of pyloric atresia compared with published literature is being reported. epidermolysis bullosa polyhydramnios pyloric atresia Pediatrics Surgery J V Subba Rao verfasserin aut Firdous Fatima verfasserin aut Fariha Anjum verfasserin aut In Journal of Indian Association of Pediatric Surgeons Wolters Kluwer Medknow Publications, 2004 26(2021), 6, Seite 416-420 (DE-627)461908964 (DE-600)2164528-0 19983891 nnns volume:26 year:2021 number:6 pages:416-420 https://doi.org/10.4103/jiaps.JIAPS_295_20 kostenfrei https://doaj.org/article/c555429cd392434196f36bbabc7f2fd8 kostenfrei http://www.jiaps.com/article.asp?issn=0971-9261;year=2021;volume=26;issue=6;spage=416;epage=420;aulast=Prasad kostenfrei https://doaj.org/toc/0971-9261 Journal toc kostenfrei https://doaj.org/toc/1998-3891 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 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_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 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 26 2021 6 416-420
allfieldsSound	10.4103/jiaps.JIAPS_295_20 doi (DE-627)DOAJ067610900 (DE-599)DOAJc555429cd392434196f36bbabc7f2fd8 DE-627 ger DE-627 rakwb eng RJ1-570 RD1-811 Gungi Raghavendra Prasad verfasserin aut Congenital Pyloric Atresia: Experience with a Series of 11 Cases and Collective Review 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Introduction: Pyloric atresia is a rare cause of congenital gastric outlet obstruction. It is often associated with epidermolysis bullosa (EB). Rarity and experience with 11 cases are the reason for this publication. Aims and Objectives: The aim and objective of this study is to present our experience of 11 cases of congenital pyloric atresia and correlate with available literature. Materials and Methods: This was retrospective cohort of 11 cases correlative comparative study. Data of all the 11 cases from 1982 to 2019 were collected, reviewed, and analyzed. The parameters studied included age, gender, antenatal diagnosis, postnatal diagnosis, preoperative management, intraoperative findings, postoperative course outcome, associated anomalies, and any genetic studies if done. All these parameters were compared with published data. Results: There were 11 cases in the present series with six boys and five girls. Most of them presented at varying periods from birth to day 1 of life. Eight cases of type 1 pyloric atresia, two cases of type 2 pyloric atresia, and one case of type 3 pyloric atresia constituted the cohort. Five out of 11 cases were associated with EB. Two out of six cases with isolated pyloric atresia and four out of five cases with EB died. Discussion: Congenital pyloric atresia may be isolated or associated with EB. Three varieties of pyloric atresia were described. Association with EB increases the mortality. Conclusions: Review and analysis of 11 cases of pyloric atresia compared with published literature is being reported. epidermolysis bullosa polyhydramnios pyloric atresia Pediatrics Surgery J V Subba Rao verfasserin aut Firdous Fatima verfasserin aut Fariha Anjum verfasserin aut In Journal of Indian Association of Pediatric Surgeons Wolters Kluwer Medknow Publications, 2004 26(2021), 6, Seite 416-420 (DE-627)461908964 (DE-600)2164528-0 19983891 nnns volume:26 year:2021 number:6 pages:416-420 https://doi.org/10.4103/jiaps.JIAPS_295_20 kostenfrei https://doaj.org/article/c555429cd392434196f36bbabc7f2fd8 kostenfrei http://www.jiaps.com/article.asp?issn=0971-9261;year=2021;volume=26;issue=6;spage=416;epage=420;aulast=Prasad kostenfrei https://doaj.org/toc/0971-9261 Journal toc kostenfrei https://doaj.org/toc/1998-3891 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 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_2003 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 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 26 2021 6 416-420
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Eight cases of type 1 pyloric atresia, two cases of type 2 pyloric atresia, and one case of type 3 pyloric atresia constituted the cohort. Five out of 11 cases were associated with EB. Two out of six cases with isolated pyloric atresia and four out of five cases with EB died. Discussion: Congenital pyloric atresia may be isolated or associated with EB. Three varieties of pyloric atresia were described. Association with EB increases the mortality. 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callnumber-first	R - Medicine
author	Gungi Raghavendra Prasad
spellingShingle	Gungi Raghavendra Prasad misc RJ1-570 misc RD1-811 misc epidermolysis bullosa misc polyhydramnios misc pyloric atresia misc Pediatrics misc Surgery Congenital Pyloric Atresia: Experience with a Series of 11 Cases and Collective Review
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topic_title	RJ1-570 RD1-811 Congenital Pyloric Atresia: Experience with a Series of 11 Cases and Collective Review epidermolysis bullosa polyhydramnios pyloric atresia
topic	misc RJ1-570 misc RD1-811 misc epidermolysis bullosa misc polyhydramnios misc pyloric atresia misc Pediatrics misc Surgery
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title_full	Congenital Pyloric Atresia: Experience with a Series of 11 Cases and Collective Review
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title_sort	congenital pyloric atresia: experience with a series of 11 cases and collective review
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title_auth	Congenital Pyloric Atresia: Experience with a Series of 11 Cases and Collective Review
abstract	Introduction: Pyloric atresia is a rare cause of congenital gastric outlet obstruction. It is often associated with epidermolysis bullosa (EB). Rarity and experience with 11 cases are the reason for this publication. Aims and Objectives: The aim and objective of this study is to present our experience of 11 cases of congenital pyloric atresia and correlate with available literature. Materials and Methods: This was retrospective cohort of 11 cases correlative comparative study. Data of all the 11 cases from 1982 to 2019 were collected, reviewed, and analyzed. The parameters studied included age, gender, antenatal diagnosis, postnatal diagnosis, preoperative management, intraoperative findings, postoperative course outcome, associated anomalies, and any genetic studies if done. All these parameters were compared with published data. Results: There were 11 cases in the present series with six boys and five girls. Most of them presented at varying periods from birth to day 1 of life. Eight cases of type 1 pyloric atresia, two cases of type 2 pyloric atresia, and one case of type 3 pyloric atresia constituted the cohort. Five out of 11 cases were associated with EB. Two out of six cases with isolated pyloric atresia and four out of five cases with EB died. Discussion: Congenital pyloric atresia may be isolated or associated with EB. Three varieties of pyloric atresia were described. Association with EB increases the mortality. Conclusions: Review and analysis of 11 cases of pyloric atresia compared with published literature is being reported.
abstractGer	Introduction: Pyloric atresia is a rare cause of congenital gastric outlet obstruction. It is often associated with epidermolysis bullosa (EB). Rarity and experience with 11 cases are the reason for this publication. Aims and Objectives: The aim and objective of this study is to present our experience of 11 cases of congenital pyloric atresia and correlate with available literature. Materials and Methods: This was retrospective cohort of 11 cases correlative comparative study. Data of all the 11 cases from 1982 to 2019 were collected, reviewed, and analyzed. The parameters studied included age, gender, antenatal diagnosis, postnatal diagnosis, preoperative management, intraoperative findings, postoperative course outcome, associated anomalies, and any genetic studies if done. All these parameters were compared with published data. Results: There were 11 cases in the present series with six boys and five girls. Most of them presented at varying periods from birth to day 1 of life. Eight cases of type 1 pyloric atresia, two cases of type 2 pyloric atresia, and one case of type 3 pyloric atresia constituted the cohort. Five out of 11 cases were associated with EB. Two out of six cases with isolated pyloric atresia and four out of five cases with EB died. Discussion: Congenital pyloric atresia may be isolated or associated with EB. Three varieties of pyloric atresia were described. Association with EB increases the mortality. Conclusions: Review and analysis of 11 cases of pyloric atresia compared with published literature is being reported.
abstract_unstemmed	Introduction: Pyloric atresia is a rare cause of congenital gastric outlet obstruction. It is often associated with epidermolysis bullosa (EB). Rarity and experience with 11 cases are the reason for this publication. Aims and Objectives: The aim and objective of this study is to present our experience of 11 cases of congenital pyloric atresia and correlate with available literature. Materials and Methods: This was retrospective cohort of 11 cases correlative comparative study. Data of all the 11 cases from 1982 to 2019 were collected, reviewed, and analyzed. The parameters studied included age, gender, antenatal diagnosis, postnatal diagnosis, preoperative management, intraoperative findings, postoperative course outcome, associated anomalies, and any genetic studies if done. All these parameters were compared with published data. Results: There were 11 cases in the present series with six boys and five girls. Most of them presented at varying periods from birth to day 1 of life. Eight cases of type 1 pyloric atresia, two cases of type 2 pyloric atresia, and one case of type 3 pyloric atresia constituted the cohort. Five out of 11 cases were associated with EB. Two out of six cases with isolated pyloric atresia and four out of five cases with EB died. Discussion: Congenital pyloric atresia may be isolated or associated with EB. Three varieties of pyloric atresia were described. Association with EB increases the mortality. Conclusions: Review and analysis of 11 cases of pyloric atresia compared with published literature is being reported.
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title_short	Congenital Pyloric Atresia: Experience with a Series of 11 Cases and Collective Review
url	https://doi.org/10.4103/jiaps.JIAPS_295_20 https://doaj.org/article/c555429cd392434196f36bbabc7f2fd8 http://www.jiaps.com/article.asp?issn=0971-9261;year=2021;volume=26;issue=6;spage=416;epage=420;aulast=Prasad https://doaj.org/toc/0971-9261 https://doaj.org/toc/1998-3891
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Eight cases of type 1 pyloric atresia, two cases of type 2 pyloric atresia, and one case of type 3 pyloric atresia constituted the cohort. Five out of 11 cases were associated with EB. Two out of six cases with isolated pyloric atresia and four out of five cases with EB died. Discussion: Congenital pyloric atresia may be isolated or associated with EB. Three varieties of pyloric atresia were described. Association with EB increases the mortality. 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Congenital Pyloric Atresia: Experience with a Series of 11 Cases and Collective Review

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