Results 91 to 100 of about 1,256,915 (264)

Robot-assisted distal gastrectomy with lymph node dissection for gastric cancer in a patient with situs inversus partialis: a case report with video file

open access: yesSurgical Case Reports, 2018
Background Situs inversus is a rare congenital condition that is currently classified into two types: complete situs inversus (situs inversus totalis, SIT) and partial situs inversus (situs inversus partialis, SIP).
Yuki Aisu   +5 more
doaj   +1 more source

Laparoscopic cholecystectomy for left-sided gall bladder in situs inversus totalis patient, a technically demanding procedure

open access: yesAnnals of Medicine and Surgery, 2019
Situs inversus is a condition in which the anatomical viscera are placed in a reverse anatomical location, it may be partial affecting the thoracic organs or the abdominal organs, or total affecting both.
A. Mohammed, S. Arif
semanticscholar   +1 more source

A twin study of cilioretinal arteries, tilted discs and situs inversus [PDF]

open access: yes, 2018
PURPOSE: To establish the prevalence and heritability of cilioretinal arteries (CRAs), tilted discs (TDs) and situs inversus (SI). METHODS: Fundus photos from the Twins UK Adult Twin registry twin database were analyzed: 1812 individuals, 526 complete ...
Baneke, AJ   +4 more
core  

A systems-biology approach to understanding the ciliopathy disorders. [PDF]

open access: yes, 2011
'Ciliopathies' are an emerging class of genetic multisystemic human disorders that are caused by a multitude of largely unrelated genes that affect ciliary structure/function.
Gleeson, Joseph G, Lee, Ji Eun
core   +1 more source

Yield of Whole Genome Sequencing for Pathogenic Single Nucleotide Variants in Congenital Heart Disease: A Systematic Review and Meta‐Analysis

open access: yesPrenatal Diagnosis, Volume 46, Issue 5-6, Page 780-818, May 2026.
ABSTRACT Objective This systematic review and meta‐analysis aimed to assess the diagnostic yield of pathogenic or likely pathogenic (P/LP) single nucleotide variants (SNVs) using whole genome sequencing (WGS) in congenital heart disease (CHD). Methods A systematic search of three databases (2000–2024) was conducted, and two reviewers independently ...
Hiba J. Mustafa   +7 more
wiley   +1 more source

Situs inversus

open access: yesCanadian Journal of Medical Sonography, 2017
Situs inversus and heterotaxy syndromes are rare and often complicated conditions that involve an abnormal arrangement of the thoracic and abdominal organs. Congenital heart defects and other complications are often present with these conditions. There is no corrective surgery recommended or available, other than for the specific cardiac anomalies ...
openaire   +2 more sources

[Situs inversus totalis].

open access: yesRevista de gastroenterologia del Peru : organo oficial de la Sociedad de Gastroenterologia del Peru, 2013
Situs inversus totalis (SIT) is a rare disease in which there is transposition of thoracic and abdominal organs. The symptoms of appendicitis in SIT are often confused with other intraperitoneal processes such as diverticulitis. We report the case of a 65-year-old, attended by emergency epigastric pain of 20 hours of the onset after a few hours left ...
Navarro, Veronica   +3 more
openaire   +4 more sources

Laparoscopic cholecystectomy in situs inversus totalis: Case report with review of techniques

open access: yesInternational journal of surgery case reports, 2019
Highlights • SIT is a rare congenital anatomy with mirror image transposition of the viscera.• The underlying anatomical variation poses a challenge in the diagnosis and management of cholelithiasis In patient with SIT.• Laparoscopic cholecystectomy can ...
Omar Alkhlaiwy   +3 more
semanticscholar   +1 more source

Fetal heterotaxy with tricuspid atresia, pulmonary atresia, and isomerism of the right atrial appendages at 22 weeks. [PDF]

open access: yes, 2013
We report the accurate prenatal diagnosis at 22 weeks gestation of right atrial isomerism in association with tricuspid atresia. Several distinctive sonographic features of isomerism of the right atrial appendages were present in this fetus: complex ...
Richardson, Randy R   +3 more
core   +2 more sources

Early Life Disease Burden and Outcomes in Children Diagnosed With Primary Ciliary Dyskinesia in Infancy

open access: yesPediatric Pulmonology, Volume 61, Issue 5, May 2026.
ABSTRACT Background Primary ciliary dyskinesia (PCD) is a genetically heterogeneous disorder causing chronic oto‐sino‐pulmonary disease from birth. Since diagnosis is often delayed into childhood or adulthood, early‐life disease burdens remain poorly described.
Madhan Kumar   +7 more
wiley   +1 more source

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