Results 61 to 70 of about 1,222,131 (133)

Polysplenia Syndrome: A Rare Case Report with Computerized Tomography Findings

, 2010
Polysplenia syndrome is a congenital anomaly in which cardiac, vascular, and thoracic anomalies are seen together. The diagnosis is mostly made in the childhood with radiological examinations which are performed due to cardiac complaints. On direkt X-ray
AVCU, Serhat, Arslan, Harun, Unal, Ozkan
core   +1 more source

Outcomes of Cardiac Repair in Heterotaxy Syndrome Patients—Tertiary Center Experience

CJC Pediatric &Congenital Heart Disease, Volume 5, Issue 1, Page 12-19, February 2026.
Abstract Background This study aims to determine factors associated with poor outcomes and frequency of arrhythmia incidence in patients with heterotaxy syndrome (HS). Methods A retrospective cohort study in a single tertiary center was conducted and included patients with operated HS between 2011 and 2020.
Mohammad A. Ebrahim, Nada T. Alzayed, Sakeena M. Alsahhaf, Mohammad A. Almulla, Karim M. Yassin, Leina A. Shabaan, Moustafa A. Elsayed, Vadim G. Lyubomudrov   +7 more
wiley   +1 more source

Heterotaxy syndrome with polysplenia: case report [PDF]

Heterotaxy syndrome (HS) or situs ambiguus is a rare condition, more common in women, in which internal organs are abnormally arranged within the thoracic and abdominal cavities. The condition may manifest as asplenia or polysplenia, characterized by the
Moreira, Sarah Verdan, Marcos, Vinícius Neves, Scapim, Stephania Neves, Ferreira, Priscila Rizutti   +3 more
core   +1 more source

An Unusual Case of Heterotaxy and Polysplenia Syndrome Associated with Hemiazygous Continuation of the Left-sided Vena Cava Inferior, Dilated Azygous Vein and Large Venous Ectasia

, 2011
We report a 13-year-old male patient with heterotaxy and polysplenia syndrome associated with hemiazygous continuation of the left-sided vena cava inferior, dilated azygous vein, and large venous ectasia.
Yildirim, Ayse, Rana Olguntürk, Olgunturk, Rana, Oner, Yusuf, Deniz Oğuz, Oguz, Deniz, Ayşe Yildirim, Yusuf Öner   +7 more
core   +1 more source

Haploinsufficiency of the FOXA2 associated with a complex clinical phenotype

Molecular Genetics & Genomic Medicine, 2020
Background There are few reports describing the proximal deletions of the short arm of chromosome 20, making it difficult to predict the likely consequences of these deletions.
Idris Mohammed, Sara Al‐Khawaga, David Bohanna, Abdusamea Shabani, Faiyaz Khan, Donald R. Love, Zafar Nawaz, Khalid Hussain   +7 more
doaj   +1 more source

Bilateral Anophthalmia Associated With Ventricular Septal Defect, Atrial Septal Defect, and Patent Ductus Arteriosus: A Rare Neonatal Case Report

Case Reports in Pediatrics, Volume 2026, Issue 1, 2026.
Background Anophthalmia is a rare congenital ocular malformation characterized by the complete absence of the eye and its associated ocular structures. Bilateral anophthalmia is particularly uncommon and is frequently associated with multisystem congenital anomalies.
Abdullahi Ali Roble, Abdisalam Ismail Hassan, Said Abdi Mohamed, Hassan Muhumed Mohamed, Ishak Ahmed Abdi, Abdijalil Abdullahi Ali, Balqiz Mohamed Kulle, Ahmed Shafie Aden, Hanan Hassan Hirei Abdalla, Mohamed Osman Dahir Alasow, Shuayb Abdullahi Adan, Ahmed Muhamad Bashir, Baisakhi Banerjee   +12 more
wiley   +1 more source

Incidental Diagnosis of Situs Inversus Totalis in a 45‐Year‐Old Male Who Presented With Acute Asthma Exacerbation: A Case Report and Brief Literature Review

Clinical Case Reports, Volume 13, Issue 11, November 2025.
ABSTRACT Incidental situs inversus totalis (SIT) requires thorough anatomical mapping to exclude associated syndromes (e.g., Kartagener) and congenital anomalies. Early identification, patient education on mirrored anatomy, and multidisciplinary coordination are essential to prevent iatrogenic errors during future interventions, even in asymptomatic ...
Ragasa Getachew Bayisa, Lensa Million Baharu, Mohammed Mecha Abafogi, Yosef Bekele Bonsa, Mohammed Kedir Shukri, Tamirat Godebo Woyimo   +5 more
wiley   +1 more source

Massive Hemoptysis in a Patient With Eisenmenger Syndrome, Polysplenia and Transverse Liver

Clinical Case Reports, Volume 13, Issue 3, March 2025.
ABSTRACT Hemoptysis is defined as blood‐streaked sputum from the lower parts of the respiratory tract. Hemoptysis, even in small amounts, is a frightening and alarm sign for possible underlying conditions such as infections, pulmonary diseases, neoplastic conditions, cardiovascular alterations, vasculitis, traumatic events, hematological derangements ...
Mohsen Shafiepour, Behnam Dalfardi, Ali Nemati, Sina Bakhshaei, Elahenaz Parsi mood   +4 more
wiley   +1 more source

Performance of Prenatal Ultrasound Screening for the Relative Positioning of Mesenteric Vessels

Journal of Ultrasound in Medicine, Volume 44, Issue 1, Page 35-45, January 2025.
Objectives Abnormal relative positioning of the superior mesenteric artery (SMA) and vein (SMV) can lead to intestinal malrotation that predisposes to midgut volvulus. The aim of this study was to assess the prenatal ultrasound ability to visualize the relative position of SMA and SMV in normal pregnancies. Methods Prospective cohort study performed in
Jean Michel Faure, Anne Larroque‐Devigne, Dominique Forgues, Eve Mousty, Alain Couture, Nicolas Kalfa, Olivier Prodhomme, Florent Fuchs   +7 more
wiley   +1 more source

Case Report: Polysplenia Syndrome, a Wide Range of Congenital Heart Malformations in an Adult

Background: Polysplenia syndrome is a rare disease where are observed two or more spleens associated with left-sided isomerism. In this condition there are many visceral and vascular congenital malformations, including cardiac anomalies. Case summary: We
Reginelli A., Giordano D. S., Cruz C., Vasconcelos M., Balestrucci G., Rebelo J., Carvalho A., Roccatagliata P.   +7 more
core   +1 more source