Results 71 to 80 of about 586,789 (263)

Congenital Lumbar Hernia with VACTERL Anomaly: A Rare Presentation [PDF]

open access: yesIndian Journal of Neonatal Medicine and Research, 2015
Congenital lumbar hernia also known as Lumbocostovertebral syndrome comprises various skeletal abnormalities like hemivertebrae, rib defects, abdominal wall anomalies and abdominal muscle hypoplasia.
Mohd. Aamir   +4 more
doaj   +1 more source

Development of the human bladder and ureterovesical junction. [PDF]

open access: yes, 2018
The urinary bladder collects urine from the kidneys and stores it until the appropriate moment for voiding. The trigone and ureterovesical junctions are key to bladder function, by allowing one-way passage of urine into the bladder without obstruction ...
Baskin, Laurence   +6 more
core   +1 more source

Therapeutic Value of Lactobacillus gasseri 345A in Chronic Constipation

open access: yesNeurogastroenterology &Motility, Volume 37, Issue 5, May 2025.
Preclinical studies show Lactobacillus gasseri to increase intestinal motility and counteract capsaicin‐stimulated transient receptor potential vanilloid 1. In a clinical trial, Lactobacillus gasseri reduced abdominal pain, along with a correlation for increased complete spontaneous bowel movements.
Stefan Roos   +7 more
wiley   +1 more source

An Extended Phenotype of PPP1R13L Cardiocutaneous Syndrome

open access: yesAmerican Journal of Medical Genetics Part A, Volume 197, Issue 4, April 2025.
ABSTRACT Dilated cardiomyopathy (DCM) is a rare disease in children and a leading cause of heart failure. There are numerous causes of DCM including genetic causes leading to isolated or syndromic presentations, with a wide variety of implicated genes.
Alicia Coudert   +8 more
wiley   +1 more source

Сочетанная патология у детей с аноректальными пороками развития (RUS) [PDF]

open access: yesСаратовский научно-медицинский журнал, 2007
The study was undertaken to review the incidence and types of associated congenital anomalies in patients with anorectal malformations (ARM ...
Morozov D.A.   +2 more
doaj  

Kabuki Syndrome and Anorectal Malformations: Implications for Diagnosis and Treatment

open access: yesEuropean Journal of Pediatric Surgery Reports, 2015
Kabuki syndrome (KS) is a rare genetic condition characterized by a distinctive facies, intellectual disability, growth delay, and a variety of skeletal, visceral, and other anomalies, including anorectal malformations (ARMs).
Sotirios Siminas   +2 more
doaj   +1 more source

Spinal cord anomalies in patients with anorectal malformations without severe sacral abnormalities or meningomyelocele: outcomes after expectant, conservative management.

open access: yesJournal of Neurosurgery : Spine, 2016
OBJECTIVE The goal of this study was to determine the significance of spinal cord anomalies (SCAs) in patients with anorectal malformations (ARMs) by comparing the outcomes for bowel function, lower urinary tract symptoms (LUTS), and lower-limb ...
K. Kyrklund   +4 more
semanticscholar   +1 more source

Pop‐off mechanisms in fetal megacystis: extravasation, umbilical cord cyst, ureterocele and megaureter

open access: yesUltrasound in Obstetrics &Gynecology, Volume 65, Issue 4, Page 487-494, April 2025.
ABSTRACT Objective To analyze comprehensively the incidence, antenatal ultrasound characteristics and prognostic implications of antenatal pop‐off mechanisms of the fetal urinary system in pregnancies with suspected fetal megacystis. Methods This was a retrospective multicenter study of pregnancies with suspected fetal megacystis conducted across all ...
L. A. M. Brinkman   +9 more
wiley   +1 more source

The Persistent Cloaca

open access: yesNational Board of Examinations Journal of Medical Sciences
Normally, at birth, females have separate perineal orifices for the urinary, reproductive and digestive tracts, while males have individual openings for the urogenital and digestive tracts.
Jayant Radhakrishnan   +3 more
doaj   +1 more source

Anorectal malformations

open access: yesJournal of Indian Association of Pediatric Surgeons, 2015
Anorectal malformations (ARMs) are among the more frequent congenital anomalies encountered in paediatric surgery, with an estimated incidence ranging between 1 in 2000 and 1 in 5000 live births. Antenatal diagnosis of an isolated ARM is rare. Most cases
Ajay Narayan Gangopadhyay   +1 more
doaj   +1 more source

Home - About - Disclaimer - Privacy