Готові списки джерел за темами / Hirshsprung Disease

Добірка наукової літератури з теми "Hirshsprung Disease"

Автор: Grafiati
Опубліковано: 10 грудня 2022
Оновлено: 28 січня 2023

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Статті в журналах з теми "Hirshsprung Disease"

1

Stockman, J. A. "Diagnostic Tests in Hirshsprung Disease: A Systematic Review." Yearbook of Pediatrics 2008 (January 2008): 173–75. http://dx.doi.org/10.1016/s0084-3954(08)70373-7.

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2

Gad El-Hak, NabilA, MohamedM El-Hemaly, EmadH Negm, EhabA El-Hanafy, MagdyH AbdEl Messeh, and HalaH AbdEl Bary. "Functional outcome after swenson′s operation for hirshsprung′s disease." Saudi Journal of Gastroenterology 16, no. 1 (2010): 30. http://dx.doi.org/10.4103/1319-3767.58765.

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3

Sohrab, Saba, Talha Shabbir, Rubina Kousar, Sadam Hussain, Quratulain Siddique, and Saleem Ahmed Khoso. "Major Congenital Malformations of Gastrointestinal Tract Among Neonates Presenting to Tertiary Care." Pakistan Journal of Medical and Health Sciences 16, no. 7 (July 30, 2022): 755–57. http://dx.doi.org/10.53350/pjmhs22167755.

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Анотація:
Background: Major congenital malformations of gastrointestinal tract (CMGIT), are usually manifested in early neonatal period by signs of intestinal obstruction and may be life threatening. A broad spectrum of Gastrointestinal Tract (GIT) anomalies can be seen including both upper and lower GIT. As compared to other congenital anomalies, GIT anomalies are not well studied and till now very few studies have reported prevalence and pattern of GIT malformations. Objective: To determine different type of common gastrointestinal anomalies among neonates presenting at tertiary care hospital. Methods: This descriptive cross sectional study was done at National Institute of Child Health (NICH) Karachi over period of 6 months, from 1-8-17 to 31-1-18. All neonates presenting to emergency department and got hospitalized with CMGIT were enrolled. Results: There were 35 neonates enrolled with CMGIT. Out of these 16(45.7%) were male and 19(54.3%) were females. Mean age 9.4+3.82 (range 1-20) days. Mean weight was 2.5±0.98 (range 0.5-4.5) kg. Mean duration of symptoms was 5.8+1.72 (range 1-9) days. Among the CMGIT, 12 (34.3%) cases were of Anorectal malformation, persistent Vitelline duct was found in 6 (17.1%), Intestinal atresia in 4(11.4%), Intestinal stenosis in 5(14.3%), Hirshsprung disease in 4(11.4%) and Exomphalos in 4 (11.4%). Conclusion: Anorectal malformations were most common anomaly followed by persistent vitelline duct. Antenatal follow up and anomaly scan of all neonates should be done. Keywords: Gastrointestinal anomaly, Neonates, congenital anomaly.
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4

Choi, Seung Hoon. "Postoperative Problems of Hirshsprung's Disease and It's Management." Journal of the Korean Association of Pediatric Surgeons 8, no. 1 (2002): 64. http://dx.doi.org/10.13029/jkaps.2002.8.1.64.

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5

Haseeb, Ahmed A., Shadi Okasha, and Atef Elbarawi. "Multifocal necrotizing fasciitis following Hirshsprung’s disease surgery away from the surgical wound site." Annals of Pediatric Surgery 11, no. 2 (April 2015): 159–61. http://dx.doi.org/10.1097/01.xps.0000462930.03634.9f.

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6

Chanchlani, Roshan, and Dhirendra Shrivastava. "Indications and complications of colostomy in newborn: our experience." International Surgery Journal 7, no. 1 (December 26, 2019): 194. http://dx.doi.org/10.18203/2349-2902.isj20195968.

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Background: The aim of the present study was to evaluate the indications, complications and outcome of colostomy in newborn patients.Methods: This is a descriptive, retrospective study carried out in the Department of Pediatric surgery, Gandhi Medical College Bhopal to evaluate acceptance and outcome of colostomy in newborn over a one year period from March 2018 to March 2019. All newborn with diagnosis of anorectal malformation, Hirshsprungs disease and other emergency conditions underwent transverse loop colostomy by expert and trained pediatric surgeon.Results: Out of 40 patients operated complications of colostomy was seen in 18 (45%) patients. Most common complication was skin excoriation in 08 patients (20%), bleeding from stoma site in 02 (05%) cases. Stoma prolapse occurred in 02 (05%) patients. Wound infection, dehiscence, stomal stenosis and parastomal hernia was seen in one patient each 2 (2.5%). 2 (0.5%) patient died due to multiple congenital anomalies.Conclusions: Colostomy in children is associated with significant morbidity in developing country. To minimize these problems, the pediatric surgeon should focus on the management and early closure of a colostomy.
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7

Fahmy, Mohammed Abd El Baky, Sameh Abd El Hay Abd El Hamid, Omar Mohammed Elsamahy, and Hanan Mahmoud Mohammed. "Comparative study between transanal endorectal pull-through and modified Duhamel’s procedure in management of Hirshsprung’s disease." Egyptian Journal of Hospital Medicine 74, no. 3 (January 1, 2019): 679–83. http://dx.doi.org/10.21608/ejhm.2019.23799.

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8

"Outcome of Laparoscopic Assisted Endorectal Pull through Versus Trans Anal Approach in Management of Hirshsprung Disease." Indian Journal of Public Health Research & Development, April 24, 2020. http://dx.doi.org/10.37506/ijphrd.v11i4.5019.

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9

Hanumaiah, Ravikumar. "A Case of Right Sided Fixation of Sigmoid Colon in a Pediatric Patient with Late onset Hirshsprung’s Disease." Clinical Radiology & Imaging Journal 5, no. 1 (2021). http://dx.doi.org/10.23880/crij-16000187.

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Дисертації з теми "Hirshsprung Disease"

1

Croaker, Geoffrey David Hain. "Clinical and Molecular Biological Studies in Hirschsprung's Disease." University of Sydney. Paediatrics and Child Health, 2002. http://hdl.handle.net/2123/520.

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Анотація:
HSCR has been felt to be a polygeneic disease on the basis of an incompletely penetrant sex modified transmission, which may be either autosomal dominant or recessive in different kindred. During the 1990's several of the genes involved in this transmission have come to light. Other genes remain to be discovered.
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Книги з теми "Hirshsprung Disease"

1

Publications, ICON Health. The Official Parent's Sourcebook on Hirshsprung's Disease: A Revised and Updated Directory for the Internet Age. Icon Health Publications, 2002.

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