This review examines the relationship between visceral and brain asymmetry and explores whether their alignment observed in some vertebrate species also exists in humans. While the development of visceral and brain asymmetry may have occurred for different reasons, it is possible that the basic mechanisms for left-right differentiation of the visceral system were duplicated in the brain. We describe the main phenotypical anomalies and the general mechanism of left-right differentiation in vertebrates, followed by a systematic review of available human studies on behavioral and brain asymmetry in individuals with reversed visceral organization. The available evidence shows no direct link between human visceral and brain laterality. Most individuals with situs inversus totalis (SIT) show typical population biases for handedness and brain functional asymmetry, although an increased prevalence of atypical hemispheric segregation may be present. Perisylvian brain structural asymmetries also reveal the expected population bias in participants with SIT. However, several independent studies indicate that SIT is associated with a general reversal of the gross morphologic asymmetry of brain torque. Potential differences in brain structural and functional asymmetries between subtypes of situs inversus with ciliary and nonciliary causes remain to be determined.
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http://dx.doi.org/10.1016/B978-0-443-15646-5.00022-1 | DOI Listing |
Handb Clin Neurol
March 2025
Department of Experimental Clinical and Health Psychology, Ghent University, Ghent, Belgium. Electronic address:
This review examines the relationship between visceral and brain asymmetry and explores whether their alignment observed in some vertebrate species also exists in humans. While the development of visceral and brain asymmetry may have occurred for different reasons, it is possible that the basic mechanisms for left-right differentiation of the visceral system were duplicated in the brain. We describe the main phenotypical anomalies and the general mechanism of left-right differentiation in vertebrates, followed by a systematic review of available human studies on behavioral and brain asymmetry in individuals with reversed visceral organization.
View Article and Find Full Text PDFJ Surg Case Rep
March 2025
Department of Vascular Surgery, Peking University People's Hospital, State Key Laboratory of Vascular Homeostasis and Remodeling, Peking University, No. 11, Xizhimen South Street, Xicheng District, Beijing 100044, PR China.
Situs inversus totalis (SIT) is a rare congenital condition characterized by mirror image transposition of thoracic and abdominal organs. The coexistence of SIT and abdominal aortic aneurysm presents unique anatomical and surgical challenges. We reported a case of a 60-year-old male with SIT and a history of endovascular aneurysm repair who developed multiple endoleaks (T1bEL, T2EL, and T3EL).
View Article and Find Full Text PDFMethodist Debakey Cardiovasc J
March 2025
Indira Gandhi Medical College, Shimla, India.
Incidental detection of polysplenia associated with situs inversus totalis in an adult is rarely reported in literature.12 "Heterotaxy" refers to a wide spectrum of anomalies involving dysmorphism of thoracoabdominal organs across the right-left axis of the body. Polysplenia is observed in left isomerism along with bilateral bilobed bronchi and bilateral morphologic left atria.
View Article and Find Full Text PDFKurume Med J
March 2025
Division of Gross and Clinical Anatomy, Department of Anatomy, Kurume University School of Medicine.
We encountered a case of situs inversus totalis in conjunction with an anomalous artery connecting the common hepatic artery and a jejunal branch of the superior mesenteric artery during anatomical dissection of a cadaver. The heart was located in the center of the thorax, with the apex located anterioinferiorly to the right of the midline and the base located posterosuperiorly to the left of the midline. The aortic arch coursed from right anterior to right posterior.
View Article and Find Full Text PDFInt J Surg Case Rep
March 2025
Department of Thoracic Surgery, Damascus Hospital, Damascus, Syria.
Introduction And Significance: Kartagener syndrome is a primary ciliary dyskinesia disorder characterized by the classic triad of chronic sinusitis, bronchiectasis, and situs inversus. The clinical presentation and age of diagnosis of this syndrome are variable, and patients require meticulous care, including antibiotics and respiratory therapy, to prevent deterioration of pulmonary function.
Case Presentation: We present the case of a female patient with a history of recurrent respiratory infections since birth, treated with antibiotics and complicated by middle ear disease.
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