Results 71 to 80 of about 4,863,546 (170)

Hirschsprung’s Disease: A Rare Adult Diagnosis [PDF]

, 2020
Case Presentation: Approximately 94% of patients with Hirschsprung’s disease (HD) are diagnosed before the age of five. In our case, a young adult with years of constipation presented to the emergency department with significant abdominal distention.
Theiling, B. Jason, McGaig, Gaea, Schmutz, Kaitlyn   +2 more
core   +1 more source

Chronic Intestinal Failure During the Neonatal Period Related to Height at Five Years of Age

Acta Paediatrica, Volume 115, Issue 8, Page 1774-1784, August 2026.
ABSTRACT Aim To clarify if children with chronic intestinal failure during the neonatal period had a different height at 5 years of age compared to standardised Swedish growth charts. Methods This retrospective cohort study of children with chronic intestinal failure during the neonatal period in Gothenburg between 2004 and 2018.
Johanna Mårtenson, Helena Borg, Julius Kristjansson, Anton Holmgren, Nils Ekvall, Anders Elfvin   +5 more
wiley   +1 more source

VALIDITAS PEMERIKSAAN KLINIS PRE-OPERASI UNTUK DIAGNOSA ENTEROKOLITIS PADA PENDERITA HIRSCHSPRUNG’S DISEASE DI RUMAH SAKIT dr. MOEWARDI - SURAKARTA [PDF]

, 2015
ABSTRAK Validitas Pemeriksaan Klinis Pre-Operasi Untuk Diagnosa Enterokolitis Pada Penderita Hirschsprung’s Disease di Rumah Sakit dr. Moewardi – Surakarta Latar Belakang : Enterokolitis merupakan komplikasi yang paling sering antara 15% – 18% pada ...
Putra, Rodijaya
core  

Pathways systematically associated to Hirschsprung’s disease

, 2013
Despite it has been reported that several loci are involved in Hirschsprung’s disease, the molecular basis of the disease remains yet essentially unknown. The study of collective properties of modules of functionally-related genes provides an efficient
Antiñolo Gil, Guillermo, Bleda, Marta, García-Alonso, Luz, Arnold, Stacey, Borrego, Salud, Luzón-Toro, Berta, Sribudiani, Yunia, Fernández, Raquel María   +7 more
core   +1 more source

Patient Demographic and Clinical Characteristics of Hirschsprung’s Disease with or without Enterocolitis.

, 2016
Patient Demographic and Clinical Characteristics of Hirschsprung’s Disease with or without Enterocolitis.
Zhoulonglong Xie (3108372), Li Hong (426614), Yi Feng (29944), Valeriy Poroyko (242930), Yuqing Li (28192), Zhilong Yan (3108375), Liya Pan (3108381), Peihua Zhao (3108378)   +7 more
core   +1 more source

Neural crest and Hirschsprung’s disease

, 2012
Neural crest cells are a transient population of stem cells in vertebrates that give rise to the entire peripheral nervous system (PNS) as well as various non-neural progenies.
Tam, PKH, Chow, KHM, Ngan, ESW
core   +1 more source

COLON ATRESIA IN COMBINATION WITH HIRSCHSPRUNG’S DISEASE: A RARE CLINICAL CASE [PDF]

, 2019
Introduction. Hirschsprung’s disease is a congenital anomaly characterized by the absence of ganglion cells in submucosal and intramuscular layers of intestinal wall that leads to the intestinal obstruction. 70–80 % of cases are isolated malformation but
A. N. Kotin, S. A. Karavaeva, A. V. Kagan, T. V. Kesaeva   +3 more
core   +1 more source

The blood serum acetylcholinesterase levels pre- and post-resection in patients with Hirschsprung’s disease

Zdorovʹe Rebenka
Background. Hirschsprung’s disease is one of the most common neonatal obstruction diseases. The annual cases of Hirschsprung’s disease in Indonesia are approximately 1,400 live births. Its screening and diagnosis can be established using several methods,
Illona Okvita Wiyogo, IGB Adria Hariastawa, Munawaroh Fitriah, Fendy Matulatan   +3 more
doaj   +1 more source

The Hirschsprung's-multiple endocrine neoplasia connection

Clinics, 2012
The risk of patients with Hirschsprung's disease later developing multiple endocrine neoplasia remains a matter of concern. The multiple endocrine neoplasia 2-Hirschsprung's disease association has been shown to cosegregate in Hirschsprung's disease ...
Sam W. Moore, Monique Zaahl
doaj   +1 more source

Early Detection and Intervention for Hirschsprung’s Disease: A Key to Successful Outcomes [PDF]

Clin Med Insights Case Rep
Hirschsprung’s disease is a congenital disorder characterized by the absence of nerve cells in the colon muscles, leading to difficulties in evacuating stool.
Rathi K, Verma A, Pingat P.
europepmc   +2 more sources