Results 71 to 80 of about 11,183 (212)

Diagnostic Challenges and Clinical Management of Area Postrema Syndrome: A Case Report on Persistent Nausea and Vomiting

open access: yesClinical Case Reports, Volume 14, Issue 7, July 2026.
ABSTRACT Area postrema syndrome (APS) is a rare neurological syndrome that presents a significant diagnostic challenge due to its nonspecific clinical manifestations, most commonly persistent nausea and vomiting, which frequently lead to initial misdiagnosis as a gastrointestinal disorder.
Andreea‐Gabriela Manole   +4 more
wiley   +1 more source

Consideration of pyloric stenosis as a cause of feeding dysfunction in children with cyanotic heart disease

open access: yesAnnals of Pediatric Cardiology, 2017
Feeding difficulty has been reported at a higher incidence in infants with cyanotic heart disease and single ventricle physiology necessitating specialized feeding strategies.
Nayan T Srivastava   +2 more
doaj   +1 more source

Trocarless laparoscopic pyloromyotomy with conventional instruments: Our experience

open access: yesJournal of Minimal Access Surgery, 2013
Background: The incidence of hypertrophic pyloric stenosis is approximately 1-3 per 1,000 live births. Hypertrophic pyloric stenosis is seen more often in males, with a male-to female ratio of 4:1.
Sandesh V Parelkar   +7 more
doaj   +1 more source

Jejunal Web Associated With Ileo‐Ileal Intussusception in a 10‐Month‐Old Female Infant: A Rare Case Report

open access: yesClinical Case Reports, Volume 14, Issue 7, July 2026.
ABSTRACT Jejunal web is a rare cause of late‐presenting intestinal obstruction in infancy. Its association with ileo‐ileal intussusception is exceptionally uncommon. A high index of suspicion and thorough intra‐operative bowel assessment are essential for diagnosis and optimal surgical management.
Rajabu Athumani Bakari   +5 more
wiley   +1 more source

Idiopathic Hypertrophic Pyloric Stenosis - A Rare Condition Mimicking Gastric Cancer in An Older Adult

open access: yes, 2023
Idiopathic hypertrophic pyloric stenosis is a very rare entity in older adults, unlike in childhood. Although the etiology of idiopathic hypertrophic pyloric stenosis is not clear, secondary causes such as excessive healing of gastric or duodenal ulcers,
DOĞAN VARAN, HACER   +3 more
core   +1 more source

Structural and Hormonal Changes Associated With Starvation in Zambian Adult Patients With Esophageal Strictures: A Cross‐Sectional Study

open access: yesHealth Science Reports, Volume 9, Issue 7, July 2026.
ABSTRACT Background and Aims Malnutrition disorders are associated with an enteropathy characterized by villus blunting, secretory cell loss, and mucosal inflammation. To investigate the contribution of undernutrition to enteropathy we conducted a case–control study of adult patients with starvation due to benign esophageal strictures, compared with ...
Ellen Besa   +7 more
wiley   +1 more source

HYPERADRENALEMIA AND PYLORIC STENOSIS [PDF]

open access: yesThe Journal of Nervous and Mental Disease, 1920
n ...
openaire   +1 more source

Duodenal obstruction due to a preduodenal portal vein

open access: yesAfrican Journal of Paediatric Surgery, 2014
An infant presented with clinical signs and symptoms suggestive of a pyloric stenosis. On abdominal ultrasound, pyloric stenosis was excluded, and other causes for proximal duodenal obstruction, such as a duodenal web or annular pancreas, were suspected.
MNC Vilakazi   +4 more
doaj   +1 more source

CONGENITAL PYLORIC STENOSIS [PDF]

open access: yesArchives of Pediatrics and Adolescent Medicine, 1911
REVIEW OF LITERATURE Reports of post-mortem findings showing pyloric stenosis with hypertrophy of the musculature, which was believed to be congenital, are found in the literature as early as 1841. Osler and Scudder accept references even much earlier. Landerer collected reports of ten such cases in 1879.
openaire   +2 more sources

A Novel Gain‐of‐Function ITPR1 Variant Associated With a Movement Disorder Characterized by Tremor and Dystonia

open access: yesAmerican Journal of Medical Genetics Part A, Volume 200, Issue 6, Page 1261-1266, June 2026.
ABSTRACT The 1,4,5‐trisphosphate receptor type 1 (ITPR1) gene encodes an endoplasmic reticulum calcium release channel, in which loss‐of‐function mutations have been associated with spinocerebellar ataxias and related neurological phenotypes. Only one gain‐of‐function mutation in the highly conserved suppressor domain of ITPR1 has been previously ...
Emilie T. Théberge   +9 more
wiley   +1 more source

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