Results 31 to 40 of about 6,535 (174)

Laparoscopic Cholecystectomy in Situs Inversus Totalis [PDF]

Journal of Clinical and Diagnostic Research, 2014
Situs inversus totalis is a rare condition where the organs in the body is placed in the opposite side. When such patient presents with the diseases of the intra abdominal organs the diagnosis is challenging and the operative procedure to be performed ...
Raghuveer M N, Mahesh Shetty S, Sunil Kumar B B   +2 more
doaj   +1 more source

Identification of major congenital malformations based on healthcare databases in France: A proof‐of‐concept study using the epi‐meres nationwide mother–child register

British Journal of Clinical Pharmacology, EarlyView.
Abstract Aim Besides registries, healthcare databases can provide useful information for assessing the frequency of major congenital malformations (MCMs) and investigating their risk factors, particularly medication exposures. This study aimed to assess the validity of MCMs identification based on French national, comprehensive healthcare databases ...
Tom Duchemin, Lise Marty, Jérôme Drouin, Sara Miranda, Jérémie Botton, Valérie Olié, Alain Weill, Rosemary Dray‐Spira   +7 more
wiley   +1 more source

Situs inversus partialis (levocardia): an incidental discovery of an extremely rare case during the autopsy of a female with suicidal poisoning

Surgical and Experimental Pathology
Background Situs inversus is a rare congenital anomaly. In this condition, the abdominal and chest organs are positioned in reverse, a mirror image of the normal anatomical position. It is divided into two categories. 1.
Jayeshkumar Kanani, Mohammed Iliyas Sheikh   +1 more
doaj   +1 more source

Video Documentary of Situs Inversus Totalis in a Male Cadaver Module 5: Lungs and Heart

MedEdPORTAL, 2014
Situs inversus totalis is a condition in which the internal organs of the human body are transposed to opposite sides. On average, 1 in 20,000 individuals has situs inversus totalis.
Gregory Casey, Lisa Campeau
doaj   +1 more source

Idiopathic thrombocytopenic purpura in a patient with situs inversus totalis: case report and literature review

Einstein (São Paulo), 2020
Situs inversus totalis is a rare recessive autosomal congenital abnormality in which the mediastinal and abdominal organs are in a mirrored position when compared to the usual topography.
Carolina Rodrigues Dal Bo, Beatriz Piovesana Devito, Leticia Piovesana Devito, Gabriella Paes del Papa, Nelson Hamerschlak   +4 more
doaj   +2 more sources

Nanophthalmos and situs inversus totalis

Indian Journal of Ophthalmology, 2012
Nanophthalmos is characterized by short axial length, high hypermetropia, thick sclera and a normal-sized crystalline lens. Situs inversus totalis is the mirror image of the normal morphology of the thoracic and abdominal viscera. To the best of our knowledge this is the first report of a nanophthalmic patient with situs inversus totalis. Therefore, we
Şahin, Alparslan, Oltulu, Refik, Kıvrak, Ali S., Özkağnıcı, Ahmet   +3 more
openaire   +4 more sources

Zebrafish inversin mutants develop scoliosis in the absence of laterality defects

Developmental Dynamics, EarlyView.
Abstract Background Human mutations in INVERSIN are associated with nephronophthisis, variable penetrance of situs inversus and congenital heart disease. Inversin has been shown to localize to cilia and many of the patient phenotypes are attributed to disrupted cilia function.
Christopher J. Derrick, Lorraine Eley, Deborah J. Henderson, Bill Chaudhry   +3 more
wiley   +1 more source

Balloon Enteroscopy‐assisted Endoscopic Retrograde Cholangiopancreatography for Choledocholithiasis in Situs Inversus Totalis With Billroth II Reconstruction: A Case Report and Literature Review

DEN Open, Volume 7, Issue 1, April 2027.
ABSTRACT Endoscopic retrograde cholangiopancreatography (ERCP) in patients with situs inversus totalis (SIT) and Billroth II reconstruction is technically challenging because of mirror‐image anatomy, altered access to the papilla, and inverted papillary orientation.
Shuhei Shintani, Shunya Oi, Kiyohiro Saito, Erina Yoshida, Noriaki Yamashita, Atsushi Nishida, Takuji Iwashita   +6 more
wiley   +1 more source

A Novel Frameshift Variant in SPAG1 Likely Causes Primary Ciliary Dyskinesia in Cocker Spaniels in Australia

Animal Genetics, Volume 57, Issue 4, August 2026.
ABSTRACT Primary ciliary dyskinesia (PCD) is a clinical syndrome that in dogs primarily manifests as chronic respiratory disease associated with cilial malfunction. The current study employs whole‐genome sequencing and a candidate gene approach to uncover the genetic basis of PCD in three Cocker Spaniel siblings following diagnosis of their respiratory
S. E. Mead, L. E. Hambrook, R. Suryadinata, P. Robinson, C. M. Wade   +4 more
wiley   +1 more source

Situs inversus

Canadian 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