Results 61 to 70 of about 586,789 (263)

Wilms Tumor in Children With AMER1/WTX Germline Pathogenic Variants: A Multicenter Case Series

open access: yesPediatric Blood &Cancer, Volume 72, Issue 8, August 2025.
ABSTRACT Background 10–15% of children with Wilms tumor (WT) have predisposing genetic syndromes. Somatic mutations are frequently identified; however, germline pathogenic variants in AMER1 are much less prevalent and are associated with osteopathia striata with cranial sclerosis (OSCS).
Insiyah Campwala   +9 more
wiley   +1 more source

Economic Analysis of Children's Surgical Care in Low- and Middle-Income Countries: A Systematic Review and Analysis. [PDF]

open access: yes, 2016
BackgroundUnderstanding the economic value of health interventions is essential for policy makers to make informed resource allocation decisions. The objective of this systematic review was to summarize available information on the economic impact of ...
Ameh, Emmanuel A   +6 more
core   +4 more sources

Neonatal Inflammation and Feeding Disorders at 1 Year in Infants With Congenital Gastrointestinal Malformations

open access: yesActa Paediatrica, Volume 114, Issue 7, Page 1702-1708, July 2025.
ABSTRACT Aim To investigate the associations between inflammatory markers and the risk of paediatric feeding disorders (PFD) at 1 year of age in infants with congenital gastrointestinal malformations (CGMs). Methods Neonates with CGMs admitted to our NICU and prospectively followed up in our outpatient clinic were included.
Cristina Mastropietro   +7 more
wiley   +1 more source

Recent advances in MRI in the preoperative assessment of anorectal malformations

open access: yesThe Egyptian Journal of Radiology and Nuclear Medicine, 2016
Objective: To prospectively evaluate the diagnostic accuracy of triplanar 2D magnetic resonance (MR) images versus the post processing reconstructed MR images generated from a single 3D VISTA sequence in children with anorectal malformations compared ...
Rania Farouk Elsayed   +2 more
doaj   +1 more source

Oral Clefts with Associated Anomalies: Findings in the Hungarian Congenital Abnormality Registry [PDF]

open access: yes, 2005
BACKGROUND: Over the years, great efforts have been made to record the frequency of orofacial clefts in different populations. However, very few studies were able to account for the etiological and phenotypic heterogeneity of these conditions. Thus, data
Czeizel, Andrew E.   +2 more
core   +3 more sources

A congenital anterior urethrocutaneous fistula in a boy whose mother was exposed to ionizing radiations: a case report and literature review [PDF]

open access: yes, 2013
Anterior congenital urethrocutaneous fistula is a rare anomaly that may present in an isolated fashion or in association with other anomalies of the genital urinary tract or anorectal malformations.
C., Menchini   +6 more
core   +2 more sources

Defining Excellence: The First Core Set of Quality Indicators for the European Paediatric Surgical Audit on Hirschsprung's Disease Care

open access: yesActa Paediatrica, Volume 114, Issue 6, Page 1464-1477, June 2025.
ABSTRACT Aim This study aimed to develop a universally applicable core set of quality indicators for Hirschsprung's disease care through a consensus‐driven process, to standardise and improve care quality across Europe. Methods A modified Delphi method was used to achieve consensus among healthcare professionals (HPs) and patient representatives (PRs ...
Daniel Rossi   +99 more
wiley   +1 more source

Sacral agenesis: a pilot whole exome sequencing and copy number study [PDF]

open access: yes, 2016
Background: Caudal regression syndrome (CRS) or sacral agenesis is a rare congenital disorder characterized by a constellation of congenital caudal anomalies affecting the caudal spine and spinal cord, the hindgut, the urogenital system, and the lower ...
Campbell, Desmond D.   +11 more
core   +1 more source

Complex trajectories are associated with neurological impairment in infants with congenital gastrointestinal malformations aged two

open access: yesActa Paediatrica, Volume 114, Issue 5, Page 992-998, May 2025.
Abstract Aim Our aims were to describe the neurodevelopment of infants with congenital gastrointestinal malformations at 2 years of age and to investigate the association between developmental delay and complex trajectories. Methods We conducted a retrospective cohort study.
Manon Midavaine   +4 more
wiley   +1 more source

Rare association of prune belly syndrome with pouch colon

open access: yesPediatric Health, Medicine and Therapeutics, 2011
M Ragavan1, U Haripriya1, PV Pradeep1, J Sarvavinothini21Department of Endocrine Surgery, 2Department of Anaesthesia, Narayana Medical College and Superspeciality Hospital, Nellore, Andhra Pradesh, IndiaAbstract: Prune belly syndrome is a triad ...
M Ragavan   +3 more
doaj  

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