Results 61 to 70 of about 1,898 (167)

Colecistectomía laparoscópica en situs inversus totalis

Cirugía Paraguaya, 2021
El situs inversus totalis es un raro desorden genético que se caracteriza por la transposición de los órganos tóracoabdominales en sentido sagital, brindando una imagen llamada “en espejo”. Su etiología todavía no es clara, pero se cree que se debe a una
Jessica Franco-López, José Berdejo, Miguel Ferreira-Bogado   +2 more
doaj   +1 more source

Treatment of achalasia with peroral endoscopic myotomy in situs inversus totalis

DEN Open, 2022
Peroral endoscopic myotomy (POEM) has become established as a safe, effective, and versatile minimally invasive endoscopic treatment for achalasia and other esophageal motility disorders. Situs inversus totalis is a rare congenital disorder characterized
Mary Raina Angeli Fujiyoshi, Yuto Shimamura, Yusuke Fujiyoshi, Kei Ushikubo, Yuki Shibata, Yohei Nishikawa, Masashi Ono, Haruo Ikeda, Manabu Onimaru, Haruhiro Inoue   +9 more
doaj   +1 more source

Balance Impairment, Muscle Oxygenation, and Functional Exercise Capacity in Patients With Primary Ciliary Dyskinesia

Pediatric Pulmonology, Volume 61, Issue 4, April 2026.
ABSTRACT Background and Objectives Extrapulmonary effects are observed in patients with primary ciliary dyskinesia (PCD), however, few studies have examined these manifestations, particularly regarding balance and muscle oxygenation during exercise. This study aimed to compare balance, functional exercise capacity, muscle oxygenation, respiratory and ...
Şeyma Mutlu Kayaarslan, Meral Boşnak Güçlü, Tuğba Şişmanlar Eyüboğlu, Ayşe Tana Aslan   +3 more
wiley   +1 more source

Rectal cancer with situs inversus totalis and previous malignant middle cerebral artery infarction: a case report and review of the literature

Journal of Medical Case Reports
Background Situs inversus totalis is a rare congenital condition where there is complete inversion of thoracic and abdominal organs. There is limited information on the laparoscopic treatment of rectal cancer in patients with situs inversus totalis ...
Shu-an Song, Shuai Liu, Fa-juan Li, Shi-lei Li, Xian-bin Liu, Shi-dong Wang, Jin-qiang Lv, Zhao-yang Qin   +7 more
doaj   +1 more source

Unraveling the Complexities of Kartagener's Syndrome: A Case of Bronchiectasis, Isolated Dextrocardia, and Primary Ciliary Dyskinesia in an Adult With Chronic Respiratory Symptoms

Clinical Case Reports, Volume 14, Issue 3, March 2026.
ABSTRACT Kartagener's Syndrome (KS), a rare autosomal recessive disorder and a subset of Primary Ciliary Dyskinesia (PCD), is characterized by chronic sinusitis, bronchiectasis, and, in approximately 50% of cases, situs inversus. This condition arises from genetic mutations that impair motile cilia function, leading to defective mucociliary clearance ...
Ibrahim Khalil, Sakib Abrar, Shah Tanvir Ahmed, Md. Imran Hossain   +3 more
wiley   +1 more source

Retrolaparoscopic adrenalectomy assisted by three-dimensional reconstructed digital model in a patient with situs inversus totalis

World Journal of Surgical Oncology, 2018
Background Situs inversus totalis is a relatively rare congenital anomaly. Performing the retrolaparoscopic adrenalectomy for the patient with situs inversus totalis is a skill-demanding and challenging surgical task, which has been even more rarely ...
Xiaobin Yuan, Bin Zhang, Caoyang Hu, Xuhui Zhang, Dongwen Wang   +4 more
doaj   +1 more source

Case Reports of Situs Inversus Totalis and Dextrocardia in Sprague Dawley Rats

Veterinary Sciences, 2019
Situs inversus totalis is a condition where there is a transposition of all internal organs from their normal anatomical location. This infrequent and rare congenital condition has been described in several species of mammals. Dextorcardia is a series of
Reynaldo Oliva Hernández, Jordan D. Lewicky, Nya L. Fraleigh, Hoang-Thanh Le   +3 more
doaj   +1 more source

Percutaneous Mitral Balloon Commissurotomy in an African Patient With Left‐Sided Inferior Vena Cava: A Rare Case Report

Case Reports in Cardiology, Volume 2026, Issue 1, 2026.
This case report describes a rare clinical scenario involving a 40‐year‐old Ethiopian female patient with very severe rheumatic mitral stenosis, found to have an anomalous transposition of the inferior vena cava (IVC). She successfully underwent a technically challenging percutaneous mitral balloon commissurotomy.
Mohammed Bedru Sebah, Yidnekachew Asrat Birhan, Gashaw Solela, Satabdi Datta Choudhury   +3 more
wiley   +1 more source

Infantile Bowel Obstruction in a Patient with Situs Inversus Totalis and Polysplenia: A Case Report

International Medical Case Reports Journal, 2022
Abdullahi Yusuf Ali,1 Ahmet Biyikli,1 Abdishakur Mohamed Abdi,1 Ilkay Guler2 1Department of Pediatric Surgery, Somalia Turkish Training and Research Hospital, Mogadishu, Somalia; 2General Directorate of Public Hospitals, Ministry of Health of Republic of
Yusuf Ali A, Biyikli A, Abdi AM, Guler I
doaj  

Dextrocardia in Heterotaxy Syndrome (Polysplenia Variant) in a 36‐Year‐Old Ethiopian Woman: A Case Report and Literature Review

Case Reports in Cardiology, Volume 2026, Issue 1, 2026.
Background Heterotaxy syndrome—polysplenia variant (left isomerism) with dextrocardia is a rare constellation of laterality defects characterized by left‐isomerism, multiple splenic nodules, and associated vascular and visceral anomalies. This report describes an adult Ethiopian woman who presented with nonspecific abdominal pain and was found to have ...
Kedir Negesso Tukeni, Ramadan Jemal Dekema, Mohammed Kedir Shukri, Jafer Yasin Mohammed, Michael Deyu Jima, Merid Lemma Kebede, Satabdi Datta Choudhury   +6 more
wiley   +1 more source