Results 61 to 70 of about 4,891,717 (200)
Neighborhood Economic Deprivation, Hispanic Ethnic Enclaves, and Congenital Anomalies in Texas
ABSTRACT Background Congenital anomalies are common, costly, and potentially life‐threatening. The impacts of structural determinants of health on risk for these conditions have scarcely been studied. We evaluated associations between residence in economically disadvantaged neighborhoods or Hispanic/Latino enclaves and congenital anomalies.
Jeremy M. Schraw +6 more
wiley +1 more source
Hipoalbuminemia prabedah sebagai faktor prognostik enterokolitis pascabedah penderita megakolon kongenital (Hirschsprungs disease) = Preoperative hypoalbuminemia as a prognostic factor of postoperative enterocolitis in [PDF]
Background: Hirschsprungs disease or congenital megacolon is the congenital absence of ganglion cells in the colon. The rectum is always involved and in 90% of patients the abnormality is confi ned to the rectum and sigmoid.
Rochadi
core
The roles of non-coding RNAs in Hirschsprung's disease
Hirschsprung's disease (HSCR) is a congenital disorder characterized by the absence of ganglion cells in the colon, leading to various intestinal complications.
Yang Yang +6 more
doaj +1 more source
Role of MiR-215 in Hirschsprung's Disease Pathogenesis by Targeting SIGLEC-8
Background/Aims: Hirschsprung's disease (HSCR), known as aganglionosis, is an infrequent congenital gut motility disorder characterized by absence of enteric neurons. In this study, we focus on the role of the intronic miR-215 and its host gene isoleucyl-
Hao Lei +5 more
doaj +1 more source
When CO2 sensing fails: Protective effects of sex hormones and potential mechanisms
Abstract Breathing movements driven by the brainstem rhythmogenic neural networks rely on chemosensory inputs to produce a motor output that is homeostatically adjusted to the prevailing metabolic demand. The central CO2 chemoreflex is a critical component of respiratory neural circuitry, as defects in these sensors cause hypoventilation syndromes ...
Tara A. Janes +2 more
wiley +1 more source
Neuronal subtype composition is comparable between transitional and fully ganglionic zones in children with Hirschsprung disease. Thus, our study did not support a major contribution of shifts in neuronal subtype composition to persistent postoperative bowel dysfunction. ABSTRACT Background Hirschsprung disease (HD) is characterized by aganglionosis of
C. Nebeling +5 more
wiley +1 more source
Diagnostic Scoring System of Hirschsprung's Disease in the Neonatal Period
Eighty to ninety percent of Hirschsprung's disease (HD) patients present in newborns. However, the diagnosis of HD in the neonatal period remains difficult.
Weihong Guo +3 more
doaj +1 more source
ABSTRACT Background Hybrid stage I palliation (HS1P) has developed as an alternative to the Norwood stage I palliation for neonates with hypoplastic left heart and related left‐sided obstructive lesions. HS1P is currently used in various clinical settings, such as single ventricle palliation, bridge to decision, bridge to biventricular repair, or ...
Johanna Hummel +8 more
wiley +1 more source
Oral and dental status in children with intestinal failure: A descriptive cross‐sectional study
Abstract Background Children with intestinal failure often experience feeding difficulties and complex daily care needs, yet their oral and dental health remains underexplored. We aimed to describe oral and dental health characteristics in pediatric intestinal failure.
Anat Guz‐Mark +3 more
wiley +1 more source
Little is known about how patients with anorectal malformations (ARMs), their caregivers and healthcare providers perceive and experience transition from pediatric to adult care (transition of care) in low‐ and middle‐income countries. This study aimed to explore the perceptions and experiences of young adults, adolescents, their caregivers, and ...
Leila Hartford +3 more
wiley +1 more source

