Results 51 to 60 of about 11,540 (186)

Right Sided Aortic Arch and its Rare Associations- A Case Series

International Journal of Anatomy Radiology and Surgery, 2018
Right sided aortic arch is a rare incidental anomaly in adults often asymptomatic. Most common subtype is Right Aortic Arch (RAA) with aberrant left subclavian artery. We report three cases of right sided aortic arch with multiple vascular anomalies. Two
Nidhi Aggarwa, Narender Kumar Kardam, Kushal Babu Gehlot   +2 more
doaj   +1 more source

Surgical management of congenital extrahepatic portosystemic shunt in a pony foal

Equine Veterinary Education, EarlyView.
Summary A five‐month‐old Welsh pony filly was admitted to the Veterinary Teaching Hospital of the University of Helsinki due to neurological signs. Clinicopathological findings showed elevated ammonium and bile acid levels. Computed tomography revealed an aberrant vessel originating from an enlarged splenic vein, leading to the right azygos vein ...
N. Hakonen, K. Niinistö, M. Laitinen, S. Mölsä, H. Tapio   +4 more
wiley   +1 more source

Unique Subclavian Vascular Ring Anomaly: Insights from CT Angiography

Life
Aortic arch anomalies represent a range of congenital vascular malformations resulting from disruptions in the typical embryological development of the aortic arch and its branches.
Radu Octavian Baz, Mihaly Enyedi, Cristian Scheau, Andreea Cristiana Didilescu, Radu Andrei Baz, Cosmin Niscoveanu   +5 more
doaj   +1 more source

Surgical repair for aortic dissection accompanying a right-sided aortic arch

Journal of Cardiothoracic Surgery, 2010
Aortic anomaly in which a right-sided aortic arch associated with Kommerell's diverticulum and aberrant left subclavian artery is rare. The present report describes a patient with type-B aortic dissection accompanying aortic anomalies consisting of right-
Saiki Naozumi, Iwahashi Toru, Koizumi Nobusato, Obitsu Yukio, Shigematsu Hiroshi   +4 more
doaj   +1 more source

Adult interrupted aortic arch with aortic regurgitation: Single-stage repair

Heart India, 2020
Adult patients with interruption of the aorta are an extremely rare occurrence. It is commonly associated with additional cardiovascular anomalies. Surgery is the mainstay in the management of the patients.
Chandra Prakash Srivastava, Ranajit Beeranna Naik, Sunil Sharma, Pradeep Kumar Goyal   +3 more
doaj   +1 more source

RLIM‐associated neurodevelopmental disorders: From clinical spectrum to molecular mechanisms

The FEBS Journal, EarlyView.
RLIM (RNF12) is an E3 ubiquitin ligase essential for mammalian development. Loss‐of‐function variants cause Tønne–Kalscheuer syndrome, while duplications cause Xq13 duplication syndrome, highlighting RLIM dosage sensitivity. This review summarizes the genetics, clinical features, and molecular mechanisms of RLIM‐associated disorders, integrating ...
Madison Landon, Kyra Swildens, Vera M. Kalscheuer, Cristina Gontan, Francisco Bustos   +4 more
wiley   +1 more source

Right-sided aortic arch with anomalous coronary artery origin and concomitant Stanford type A dissection: A rare case report

Radiology Case Reports
Congenital anomalies of the aortic arch are rare and may be incidentally discovered or present with life-threatening complications. We report a case of a 58-year-old man with hypertension and a remote history of smoking, who presented with sudden, severe
Giuseppe Maria Andrea D’Arma, MD, Manuela Montatore, MD, Domenico Riccardo Rosario Chieppa, MD, Federica Masino, MD, Saverio Pollice, MD, Giuseppe Guglielmi, MD   +5 more
doaj   +1 more source

A case of tracheal bronchus associated with right aortic arch and partial anomalous pulmonary venous connection

Türk Kardiyoloji Derneği Arşivi, 2016
Tracheal bronchus includes a variety of bronchial anomalies arising in the trachea or main bronchus and directed toward the upper-lobe territory. Reported incidence varies from 1–3% in the pediatric population.
Vehbı DOGAN, İlker Ertuğrul, Yasemin Taşcı Yıldız, Utku Arman Örün, Selmin Karademir   +4 more
doaj   +1 more source

Standardized Reporting of Cardiac Magnetic Resonance Examinations in Children With Cardiac Diseases and Adults With Congenital Heart Disease: A Scientific Statement From the Association for European Pediatric and Congenital Cardiology (AEPC) and the International Society for Magnetic Resonance in Medicine (ISMRM)

Journal of Magnetic Resonance Imaging, EarlyView.
Francesca Raimondi, Inga Voges, Lamia Ait‐Ali, Sonya Babu‐Narayan, Rene Botnar, Barbara Burkhardt, Adrienne Campbell‐Washburn, Dominik Daniel Gabbert, Georg Hansmann, Willem A. Helbing, Hasan Hosan, Sylvia Krupickova, Heiner Latus, Duarte Martins, Colin McMahon, Christian Meierhofer, Vivek Muthurangu, Tiina Ojala, Pim van Ooij, Claudia Prieto, Milan Prsa, Kuberan Pushparajah, José F. Rodríguez Palomares, Samir Sarikouch, Lars Grosse‐Wortman, F. Gerald Greil, Heynric Grotenhuis   +26 more
wiley   +1 more source

Cyclin‐dependent kinase 13 is indispensable for normal mouse heart development

Journal of Anatomy, Volume 246, Issue 4, Page 616-630, April 2025.
Congenital heart disease (CHD) is the most common defect in live births. The role of cyclin‐dependent kinase (CDK13) in cardiogenesis and CHD was studied using a transgenic mouse model (Cdk13tm1b) carrying deletion of exons 3 and 4, causing loss of function.
Qazi Waheed‐Ullah, Anna Wilsdon, Aseel Abbad, Sophie Rochette, Frances Bu'Lock, Asma Ali Saed, Marc‐Phillip Hitz, J. David Brook, Siobhan Loughna   +8 more
wiley   +1 more source