Zobrazeno 1 - 10
of 72
pro vyhledávání: '"Congenital microgastria"'
Publikováno v:
European Journal of Pediatric Surgery Reports, Vol 05, Iss 01, Pp e17-e20 (2017)
Abstract Microgastria is a rare congenital condition often associated with other anomalies. In the present report we describe the case of a 6-year-old girl with isolated CM who presented with dumping syndrome successfully treated by a Hunt-Lawrence p
Externí odkaz:
https://doaj.org/article/e48af0c60ab447f98e2cb39e8df8fbfa
Publikováno v:
American Journal of Medical Genetics Part A. 182:2976-2981
We report a patient with phenotypic semblance to the congenital microgastria-limb reduction association (MLRD). Our patient presented with microgastria, bilateral upper limb anomalies, asplenia, solitary kidney, and mild micrognathia. In addition to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc3eee83775e7137a8599eee6eda8340
https://doi.org/10.1002/ajmg.a.61872
https://doi.org/10.1002/ajmg.a.61872
Akademický článek
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Publikováno v:
European Journal of Pediatric Surgery Reports, Vol 05, Iss 01, Pp e17-e20 (2017)
European Journal of Pediatric Surgery Reports
European Journal of Pediatric Surgery Reports
Microgastria is a rare congenital condition often associated with other anomalies. In the present report we describe the case of a 6-year-old girl with isolated CM who presented with dumping syndrome successfully treated by a Hunt-Lawrence pouch.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3449c8d3f6c8db7c29a2980b833b807e
https://doi.org/10.1055/s-0037-1601305
https://doi.org/10.1055/s-0037-1601305
Autor:
Larissa I. A. Ruczynski, Ivo de Blaauw, Sanne M. B. I. Botden, Horst E. Daniels-Scharbatke, Maarten Schurink
Publikováno v:
European Journal of Pediatric Surgery, 31, 129-134
European Journal of Pediatric Surgery, 31, 2, pp. 129-134
European Journal of Pediatric Surgery, 31, 2, pp. 129-134
Contains fulltext : 239093.pdf (Publisher’s version ) (Closed access) INTRODUCTION: Congenital microgastria is an extremely rare birth defect. The aim of this study was to present an overview of existing literature on the treatment of microgastria.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::336fe7b5793976adfcc31db847b959df
https://pubmed.ncbi.nlm.nih.gov/32422678
https://pubmed.ncbi.nlm.nih.gov/32422678
Kniha
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Publikováno v:
Diseases of the Esophagus. 32
This study reports the case of a male infant born at full term with antenatal suspicion for esophageal atresia (EA). At birth inability to pass a feeding tube and a gasless abdomen on plain film X-ray led to the diagnosis of pure EA according to inte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e61cd18d058f3a00789e09e2dc9e29d1
https://doi.org/10.1093/dote/doz047.102
https://doi.org/10.1093/dote/doz047.102
Autor:
Othman A. Al-Johani, Mohammed Hasosah, Stanley Crankson, Ahmed A Abdul-Wahab, Mohammad Al-Namshan, Saud Al Jadaan, Abdullah Al-Rabeeah, Mohammad Zamakhshary, Omar Oda
Publikováno v:
Annals of Pediatric Surgery; Vol 7, No 3 (2011); 114-116
Congenital microgastria (CM) is an extremely rare anomaly of the caudal part of the foregut. Treatment of CM has not yet been standardized. We present the case of a 34-monthold girl with an isolated CM complicated by nasogastric tube-related gastric
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::650f722df4c7e4e213169d77da38f229
https://doi.org/10.1097/01.xps.0000399159.05940.0f
https://doi.org/10.1097/01.xps.0000399159.05940.0f
Akademický článek
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Autor:
K Ravikiran, S Pramod
Publikováno v:
International Surgery Journal. 5:1130
Microgastria is a rare congenital anamoly. It was first reported in 1800s. It occurs in association with other anamolies. Common associated anomalies include asplenia, malrotation of intestine, upper limb anomalies, situs inversus. Isolated cases of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c57027a656fedcd901746b407781381b
https://doi.org/10.18203/2349-2902.isj20180844
https://doi.org/10.18203/2349-2902.isj20180844