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Quoted phrase not found in phrase index: "Hirschsprung disease, susceptibility to, 7"
Page 1
Inflammatory bowel disease in patients with Hirschsprung's disease: a systematic review and meta-analysis.
Nakamura H, Lim T, Puri P. Nakamura H, et al. Pediatr Surg Int. 2018 Feb;34(2):149-154. doi: 10.1007/s00383-017-4182-4. Epub 2017 Oct 5. Pediatr Surg Int. 2018. PMID: 28983688 Review.
AIM AND OBJECTIVES: Hirschsprung-associated enterocolitis (HAEC) continues to be an important cause of morbidity in patients with Hirschsprung's disease (HSCR). ...MATERIALS AND METHODS: A systematic literature search for relevant articles was performed in fo …
AIM AND OBJECTIVES: Hirschsprung-associated enterocolitis (HAEC) continues to be an important cause of morbidity in patients with …
Hirschsprung's disease: genetic and functional associations of Down's and Waardenburg syndromes.
Moore SW, Johnson AG. Moore SW, et al. Semin Pediatr Surg. 1998 Aug;7(3):156-61. doi: 10.1016/s1055-8586(98)70011-3. Semin Pediatr Surg. 1998. PMID: 9718653 Review.
Despite significant advances in understanding the genetic background in Hirschsprung's disease (HD), the majority of cases are believed to be multigenic and multifactorial. ...Mutations of known genes appear to account for only a relatively small number of HD cases …
Despite significant advances in understanding the genetic background in Hirschsprung's disease (HD), the majority of cases are …
Genetic impact on the treatment & management of Hirschsprung disease.
Moore SW. Moore SW. J Pediatr Surg. 2017 Feb;52(2):218-222. doi: 10.1016/j.jpedsurg.2016.11.012. Epub 2016 Nov 13. J Pediatr Surg. 2017. PMID: 28003043 Review.
BACKGROUND: The identification of Hirschsprung's disease (HD) as a genetic condition has been a major step forward in understanding the development of the enteric nervous system and conditions arising from ganglion cell maldevelopment. METHOD: A study of the role of …
BACKGROUND: The identification of Hirschsprung's disease (HD) as a genetic condition has been a major step forward in understa …
Molecular Diagnosis and Treatment of Multiple Endocrine Neoplasia Type 2B in Ethnic Han Chinese.
Zhang ZW, Guo X, Qi XP. Zhang ZW, et al. Endocr Metab Immune Disord Drug Targets. 2021;21(3):534-543. doi: 10.2174/1871530320666200910112230. Endocr Metab Immune Disord Drug Targets. 2021. PMID: 32914730
Further, a total of 32 MEN 2B patients from literature were clustered with 28 available for analysis. 26 (92.8%) were diagnosed by endocrine-related symptoms; the remaining 2 (7.2%) due to RET testing and oral symptoms, respectively. 25 patients underwent thyroidectomy wit …
Further, a total of 32 MEN 2B patients from literature were clustered with 28 available for analysis. 26 (92.8%) were diagnosed by endocrine …
A population-based description of familial clustering of Hirschsprung disease.
Teerlink CC, Bernhisel R, Cannon-Albright LA, Rollins MD. Teerlink CC, et al. J Pediatr Surg. 2018 Jul;53(7):1355-1359. doi: 10.1016/j.jpedsurg.2017.08.024. Epub 2017 Sep 1. J Pediatr Surg. 2018. PMID: 28919319
BACKGROUND: Familial recurrence of Hirschsprung disease (HSCR) is well documented, and risk estimates for relatives have been reported from various populations. ...CONCLUSION: This population-based survey of HSCR provides confirmation of a genetic contribution to HS …
BACKGROUND: Familial recurrence of Hirschsprung disease (HSCR) is well documented, and risk estimates for relatives have been …
Trends and Predictors of Clostridium difficile Infection among Children: A Canadian Population-Based Study.
El-Matary W, Nugent Z, Yu BN, Lix LM, Targownik LE, Bernstein CN, Singh H. El-Matary W, et al. J Pediatr. 2019 Mar;206:20-25. doi: 10.1016/j.jpeds.2018.10.041. Epub 2018 Nov 15. J Pediatr. 2019. PMID: 30448272

Comorbid conditions, more prevalent among children with CDI than matched controls, included Hirschsprung disease (P < .001) and inflammatory bowel disease (P < .0001). ...CONCLUSIONS: The incidence of CDI is stable among children in Manitoba. Children w

…

Comorbid conditions, more prevalent among children with CDI than matched controls, included Hirschsprung disease (P < .001)

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WNT3A gene expression is associated with isolated Hirschsprung disease polymorphism and disease status.
Chen D, Mi J, Liu X, Zhang J, Wang W, Gao H. Chen D, et al. Int J Clin Exp Pathol. 2014 Mar 15;7(4):1359-68. eCollection 2014. Int J Clin Exp Pathol. 2014. PMID: 24817932 Free PMC article.
It has been found Wnt signaling pathway is closely related with embrionic development and Hirschsprung disease (HSCR). A common haplotype consisting of minor SNPs alleles located in the WNT3A gene has been described as a risk factor for various genetic disorders. .. …
It has been found Wnt signaling pathway is closely related with embrionic development and Hirschsprung disease (HSCR). A commo …
Cumulative Risk Impact of RET, SEMA3, and NRG1 Polymorphisms Associated With Hirschsprung Disease in Han Chinese.
Li Q, Zhang Z, Diao M, Gan L, Cheng W, Xiao P, Su L, Shangguan S, Jiang Q, Li L. Li Q, et al. J Pediatr Gastroenterol Nutr. 2017 Mar;64(3):385-390. doi: 10.1097/MPG.0000000000001263. J Pediatr Gastroenterol Nutr. 2017. PMID: 27203398
OBJECTIVES: Hirschsprung disease (HSCR) is a congenital aganglionosis of myenteric and submucosal plexuses affecting a variable length of the intestine. ...Through the assessment of risk alleles by effect size, individuals were classified into 3 weighted risk score …
OBJECTIVES: Hirschsprung disease (HSCR) is a congenital aganglionosis of myenteric and submucosal plexuses affecting a variabl …
Genotype-phenotype relationship in Japanese patients with congenital central hypoventilation syndrome.
Shimokaze T, Sasaki A, Meguro T, Hasegawa H, Hiraku Y, Yoshikawa T, Kishikawa Y, Hayasaka K. Shimokaze T, et al. J Hum Genet. 2015 Sep;60(9):473-7. doi: 10.1038/jhg.2015.65. Epub 2015 Jun 11. J Hum Genet. 2015. PMID: 26063465
In 19 cases carrying 25 PARM, the male-to-female ratio was ~3, no cases had Hirschsprung disease; 7 cases (37%) developed hypoventilation after the neonatal period, and 8 cases (42%) had mental retardation. In other 73 cases carrying 26 or more PARMs or NPARM …
In 19 cases carrying 25 PARM, the male-to-female ratio was ~3, no cases had Hirschsprung disease; 7 cases (37%) develop …
Clinical and genetic differences in total colonic aganglionosis in Hirschsprung's disease.
Moore SW, Zaahl M. Moore SW, et al. J Pediatr Surg. 2009 Oct;44(10):1899-903. doi: 10.1016/j.jpedsurg.2009.04.026. J Pediatr Surg. 2009. PMID: 19853744
Although apparently the same condition as Hirschsprung's disease (HSCR), total colonic aganglionosis (TCA) patients (2%-14% congenital aganglionosis) display clinical, histopathologic, and genetic differences that may account for altered clinical presentations. ...P …
Although apparently the same condition as Hirschsprung's disease (HSCR), total colonic aganglionosis (TCA) patients (2%-14% co …
18 results