Results 61 to 70 of about 11,531 (208)

Congenital Anomalies of Aortic Arch: A Pictorial Essay

open access: yesIndian Journal of Radiology and Imaging, 2022
Aortic abnormalities account for 15 to 20% of all congenital cardiovascular diseases. The purpose of this pictorial essay is to illustrate various congenital anomalies of the aortic arch, which influence patient management and outcome.
Archita Goel, Sanjaya Viswamitra
doaj   +1 more source

Advancing fetal autopsy in cases of maceration: Underwater dissection technique and its forensic relevance

open access: yesJournal of Forensic Sciences, EarlyView.
Abstract Fetal autopsy remains essential for determining the cause of intrauterine death and for supporting clinical, genetic, and forensic evaluations. However, in cases of advanced maceration, autolysis severely compromises tissue integrity, often preventing adequate identification of anatomical structures and limiting the diagnostic and medico‐legal
Francesca Buffelli   +4 more
wiley   +1 more source

Aortic arch interruption and persistent fifth aortic arch in phace syndrome: Prenatal diagnosis and postnatal course

open access: yes, 2015
PHACE is a rare congenital neurocutaneous syndrome where posterior fossa malformations, hemangiomas, cerebrovascular anomalies, aortic arch anomalies, cardiac defects, and eye abnormalities are variably associated.
Serranti D.   +5 more
core   +1 more source

Unique Subclavian Vascular Ring Anomaly: Insights from CT Angiography

open access: yesLife
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   +5 more
doaj   +1 more source

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

open access: yesInternational 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   +2 more
doaj   +1 more source

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

open access: yesJournal 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   +8 more
wiley   +1 more source

Left cervical aortic arch associated with multiple vascular anomalies

open access: yes, 2011
Cervical aortic arch is a rare anomaly occasionally associated with other cardiovascular abnormalities. We present a case of tortuous left cervical aortic arch associated with hypoplastic transverse arch, coarctation of the aorta, and right ...
José Luiz Balthazar Jacob
core   +1 more source

320-slice CT angiography of an interrupted aortic arch patient relying on collaterals: An addition to classification criteria

open access: yesRadiology Case Reports, 2019
A 13-year-old female patient presented with chest pain had no history of heart disease or trauma. She was finally diagnosed with the interrupted aortic arch by 320-slice CT angiography, without intracardial malformations or patent ductus arteriosus.
Peng Wang, MM   +3 more
doaj   +1 more source

Soft tissue abnormalities in the congenital limb malformation radial dysplasia (RD): Their clinical impact and treatment significance

open access: yesJournal of Anatomy, EarlyView.
We review the characteristic changes to the limb soft tissue and neurovascular abnormalities that have been described in the congenital limb birth defect, Radial Dysplasia. These include consistent changes in muscle anatomy or absence of specific muscles, persistent median arteries and absent radial arteries and consistent alterations in neural ...
Marco Correia Duarte   +6 more
wiley   +1 more source

Genomic Contributors to Congenital Diaphragmatic Hernia: Results of Exome Sequencing in 560 Probands and Cross Reference of Findings in an Independent Cohort

open access: yesAmerican Journal of Medical Genetics Part A, Volume 200, Issue 8, Page 1821-1831, August 2026.
ABSTRACT There is a strong genetic contribution to the etiology of congenital diaphragmatic hernia (CDH). This study evaluated genetic testing results and diagnostic yield for fetuses and children with CDH. This was a retrospective cohort study of exome sequencing (ES) performed at GeneDx for fetuses and children ≤ 18 years of age with CDH compared ...
Justin Blair   +9 more
wiley   +1 more source

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