Results 51 to 60 of about 45,575 (193)

Common bile duct adenocarcinoma in a patient with situs inversus totalis: report of a rare case

open access: yesBMC Research Notes, 2012
Background Situs inversus totalis represents an unusual anomaly characterized by a mirror-image transposition of the abdominal and thoracic viscera.
Benhammane Hafida   +7 more
doaj   +1 more source

Laparoscopic Cholecystectomy in Situs Inversus Totalis with Stage 5 Chronic Kidney Disease: A Case Report

open access: yesJournal of Nepal Medical Association, 2023
Situs inversus totalis is a rare congenital anomaly in which the abdominal and thoracic organs are transposed in a mirror image. Diagnosis and management of cholelithiasis in patients with situs inversus totalis pose a challenge due to the anatomical ...
Sneha Raut   +4 more
doaj   +1 more source

PIH1D2 Loss‐of‐Function Directs Ciliary and Cell Cycle Defects Resulting in Left Isomerism With or Without Biliary Atresia

open access: yesLiver International, Volume 46, Issue 11, November 2026.
ABSTRACT Background & Aims Laterality disorders are rare congenital conditions caused by disruption of left–right embryonic patterning, often associated with ciliary dysfunction. Despite the identification of numerous causative genes, the molecular basis remains unresolved in many patients.
Alina Kurolap   +19 more
wiley   +1 more source

A Backwards Approach to Bariatric Surgery: The Perioperative Approach Used in a Woman with Situs Inversus Totalis Undergoing a Laparoscopic Sleeve Gastrectomy

open access: yes, 2018
Situs inversus totalis is a rare congenital condition where organs are mirrored across the sagittal plane of the body. In the absence of associated comorbidities, most people have normal health and lifespan.
Villalvazo, Yadira, Jensen, Candice M
core   +1 more source

Making the Diagnosis of Primary Ciliary Dyskinesia in Australia

open access: yesPediatric Pulmonology, Volume 61, Issue 10, October 2026.
ABSTRACT Background and Objective Primary Ciliary Dyskinesia (PCD) is a genetic disorder associated with recurrent infections and irreversible airway damage. No single diagnostic test exists, necessitating use of a diagnostic algorithm that varies internationally.
Michelle Cai   +7 more
wiley   +1 more source

Biliary Atresia With Situs Inversus Abdominalis Managed by Kasai Portoenterostomy: A Case Report From Muhimbili National Hospital, Tanzania

open access: yesClinical Case Reports, Volume 14, Issue 9, September 2026.
ABSTRACT Biliary atresia associated with situs inversus abdominalis is a rare congenital combination that complicates diagnosis and surgical orientation. Early recognition, meticulous preoperative planning, and timely Kasai portoenterostomy can achieve favorable short‐term outcomes.
Rajabu Athumani Bakari   +7 more
wiley   +1 more source

Reporte de Caso: Situs Inversus Totalis [PDF]

open access: yes, 2018
Se presenta el caso clínico de un paciente masculino de 45 años de edad con un cuadro clínico de 15 horas de evolución caracterizado por dolor abdominal con predominio en flanco y fosa ilíaca izquierdos.
Bastidas Granizo, Leonela Carolina   +2 more
core   +3 more sources

Successful endovascular infrarenal aneurysm repair in a patient with situs inversus totalis [PDF]

open access: yes, 2010
Situs inversus totalis is a rare autosomal recessive developmental anomaly. There are very few reports in the published literature of abdominal aortic aneurysm in patient with situs inversus totalis, all of whom underwent open aneurysm repair.
Qing, KX   +7 more
core   +1 more source

Clinical Outcomes of Chronic Airway Infection in Primary Ciliary Dyskinesia

open access: yesPediatric Pulmonology, Volume 61, Issue 9, September 2026.
ABSTRACT Introduction Primary ciliary dyskinesia (PCD) is a rare disorder of impaired respiratory mucociliary clearance and chronic pulmonary infections. The clinical impact of chronic infection is poorly understood. The objective of this single‐center, retrospective cohort study was to assess clinical outcomes of people with PCD and chronic airway ...
Thomas G. Saba   +3 more
wiley   +1 more source

Systematic Reanalysis of Whole‐Exome Sequencing in Genetically Unsolved Pediatric Primary Ciliary Dyskinesia

open access: yesPediatric Pulmonology, Volume 61, Issue 8, August 2026.
ABSTRACT Background Primary ciliary dyskinesia (PCD) is a genetically heterogeneous disorder, and despite advances in next‐generation sequencing, a substantial proportion of clinically suspected pediatric cases remain without a molecular diagnosis.
Tilbe Hakçıl Öz   +4 more
wiley   +1 more source

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