Results 41 to 50 of about 1,654,151 (233)

Heterotaxy syndrome with complex congenital heart disease, facial palsy, and asplenia: A rare newborn finding

Clinical Case Reports, 2021
Heterotaxy syndrome is associated with asplenia/polysplenia and complex congenital heart disease. Facial palsy in heterotaxy is very rare. The management is still challenging with a poor prognosis. Proper counseling to the family about the disease course,
Sanjeev Kharel, Dinesh Prasad Koirala, Suraj Shrestha, Hari Sedai, Bibek Man Shrestha, Sushan Homagain, Suraj Kandel   +6 more
doaj   +1 more source

A Rare Case of Polysplenia Syndrome Associated with Severe Cardiac Malformations and Congenital Alveolar Dysplasia in a One-Month-Old Infant: A Complete Macroscopic and Histopathologic Study

Journal of Cardiovascular Development and Disease, 2022
Polysplenia syndrome represents a type of left atrial isomerism characterized by multiple small spleens, often associated with cardiac malformations and with situs ambiguus of the abdominal organs.
Cosmin Ioan Mohor, Sorin Radu Fleaca, Alexandra Oprinca Muja, George Calin Oprinca, Mihai Dan Roman, Radu Chicea, Adrian Gheorghe Boicean, Horatiu Dura, Ciprian Tanasescu, Nicolas Catalin Ionut Ion, Mihai Faur, Ciprian Ionut Bacila, Florina Batar, Calin Ilie Mohor   +13 more
doaj   +1 more source

Video Documentary of Situs Inversus Totalis in a Male Cadaver Module 1: Initial Discovery of Situs Inversus Totalis

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

Understanding laterality disorders and the left-right organizer: Insights from zebrafish

Frontiers in Cell and Developmental Biology, 2022
Vital internal organs display a left-right (LR) asymmetric arrangement that is established during embryonic development. Disruption of this LR asymmetry—or laterality—can result in congenital organ malformations.
Kadeen Forrest, Alexandria C. Barricella, Sonny A. Pohar, Anna Maria Hinman, Jeffrey D. Amack, Jeffrey D. Amack   +5 more
doaj   +1 more source

Situs Ambiguous with Intestinal Malrotation, Short Pancreas and Interruption of The Inferior Vena Cava Revealing A Polysplenia Syndrome

, 2020
Case Report Polysplenia syndrome is a rare situs ambiguous anomaly associated with multiple spleens and anomalies of chest and abdominal organs. We present a case of polysplenia syndrome found in a 11-year-old child. Radiological examinations are helpful
S. Dehbi, M. Aitchtouk, I. Zouita, D. Basraoui, H. Jalal   +4 more
semanticscholar   +1 more source

Heterotaxy Syndrome In A Middle-Aged Pakistani Male

Journal of Rawalpindi Medical College, 2023
Background: Heterotaxy syndrome (or situs ambiguous) is an extremely rare disorder in which the viscera are arranged in an abnormally asymmetrical pattern around the midline along with cardiac and spleen abnormalities.
Seema Kanwal, Ahsan Tameez ud Din, Mudassir Shafiq, Farzana Kausar, Asim Tameez Ud Din   +4 more
doaj   +1 more source

Acute appendicitis in a patient with heterotaxy syndrome

Journal of Pediatric Surgery Case Reports, 2018
Heterotaxy syndrome, also known as situs ambiguous, is a congenital condition that results in an abnormal distribution of visceral organs in the chest and abdomen. Heterotaxy syndrome has generally been categorized into two forms: a left-atrial isomerism
Mariam Selevany, Manrique Guerrero, John A. Perrone, Maryam Hussain   +3 more
doaj   +1 more source

Fluorescence in situ hybridization for ambiguous melanocytic tumors.

Histology and histopathology, 2012
The large majority of melanocytic lesions can be reliably classified as either benign or malignant based upon morphology alone, but a minority of lesions remains difficult to classify by traditional histologic methods. Recently, a panel of fluorescence in situ hybridization (FISH) probes targeting loci on chromosomes 6 and 11 has emerged as a powerful ...
Gammon, Bryan, Gerami, Pedram
openaire   +3 more sources

Situs ambiguous with duodenal atresia in a neonate: A case report with literature review

Journal of Neonatal Surgery
Background: Situs ambiguous is a rare congenital anomaly characterized by an unusual and irregular distribution of the major visceral organs and vessels within the chest and abdomen.
O. Edan
semanticscholar   +1 more source

Situs ambiguous - polysplenia syndrome type

Radiopaedia.org, 2012
Ayla Al Kabbani, M. Niknejad
openaire   +2 more sources