Results 31 to 40 of about 11,540 (186)

Longitudinal Echocardiographic Surveillance of Aortic Dilation in a Phenotype‐Enriched Turner Syndrome Cohort

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Turner syndrome (TS) is associated with thoracic aortopathy and increased risk for aortic dissection, yet the natural history of aortic dilation is not well understood. We performed a retrospective longitudinal study of individuals with TS who participated in the TS Society of the United States Healthy Heart Project between 2003 and 2023 ...
Dylan Doerner, Matthew R. Johnson, Sara Mansoorshahi, Rakesh Kathiresan, Katelyn Abel, Jonathan G. You, Emilio Quezada, Siddharth K. Prakash   +7 more
wiley   +1 more source

Laryngeal branches of the recurrent laryngeal nerve: A narrative review of human anatomical studies

The Anatomical Record, EarlyView.
Abstract The recurrent laryngeal nerve (RLN) provides motor innervation to all intrinsic laryngeal muscles except the cricothyroid. Detailed knowledge of its terminal branching is essential for thyroid, laryngeal, and voice surgeons. This review synthesizes existing human cadaveric and surgical descriptions of the extralaryngeal and motor branching of ...
Daniel Goodman, Jordan Higgs, Robert T. Sataloff   +2 more
wiley   +1 more source

Photogrammetric Reconstruction of 3D Human Anatomical Structures and Augmented Reality via Smartphone Technology

Clinical Anatomy, EarlyView.
ABSTRACT Limited access to cadavers necessitates the availability of digital resources for anatomy education. Smartphone‐based photogrammetry offers a promising solution for creating three‐dimensional (3D) and augmented reality (AR) models. This study compared two mobile photogrammetry applications (Qlone and Polycam) that have been used in modern ...
Sarita Phukwantong, Paphawarin Ma‐imjai, Benrita Jitaree, Athinan Prommahom   +3 more
wiley   +1 more source

Case Series of Berry syndrome: A rare constellation of fatal cardiac anomalies

Annals of Pediatric Cardiology, 2023
Berry syndrome is an extremely rare constellation of several congenital cardiac anomalies consisting of aortopulmonary window, aortic origin of the right pulmonary artery (AORPA), interrupted aortic arch or hypoplastic aortic arch or coarctation of the ...
Kevin Moses Hanky Jr Tandayu, Yovi Kurniawati, Indriwanto Sakidjan Atmosudigdo, Oktavia Lilyasari   +3 more
doaj   +1 more source

Secretopathies emerge as a new class of neurocristopathies

Developmental Dynamics, EarlyView.
Abstract Neural crest cells are a transient embryonic population of cells that give rise to a wide range of structures, including craniofacial cartilage and bone, peripheral neurons and glia, as well as components of the cardiac outflow tract, among others.
Amanda Teixeira, Cassandra Millet‐Boureima, Joshua A. Moore, Loydie A. Jerome‐Majewska   +3 more
wiley   +1 more source

Electroclinical phenotypes—genetic characterization of developmental and epileptic encephalopathies in a cohort study

Epileptic Disorders, EarlyView.
Abstract Objective Developmental and epileptic encephalopathies (DEEs) are characterized by refractory seizures and frequently recurring epileptic activity with neurodevelopmental delay or regression that usually begin in early life. We aimed to define the relationship between electroclinical features and etiology, as well as the genotype–phenotype ...
Burcu Yaman, Fulya Kurekci, Sinan Akbas, Ceyda Oney, Mehmet Akif Kilic, Hulya Maras Genc, Ayca Dilruba Aslanger, Edibe Pembegul Yildiz   +7 more
wiley   +1 more source

Experience of diagnosis of congenital arterial anomaly in a child with bronchial obstruction: clinical case and summary

Zdorovʹe Rebenka, 2017
Congenital anomalies of the aortic arch are a large group of cardiovascular anomalies. Some of them are isolated; others are associated with congenital heart defects or genetic syndromes. There can be different clinical manifestations of these anomalies —
L.V. Besh, O.I. Matsyura, V.B. Yaskiv, M.V. Konyk, V.F. Petrov, LV. Dvorchyn, O.V. Omelyanenko, O.V. Malko, O.V. Pasternak   +8 more
doaj   +1 more source

Combined Karyotyping, Copy Number Variation Sequencing, and Whole Exome Sequencing in the Prenatal Diagnosis of Congenital Heart Disease: Detection Rates and Phenotypic Associations

Journal of Clinical Laboratory Analysis, EarlyView.
This study combined karyotyping, copy number variation sequencing, and whole‐exome sequencing to assess the value of genetic testing in the prenatal diagnosis of congenital heart disease (CHD) and to evaluate the relationship between genetic variants and prenatal phenotypes.
Jieqiong Xie, Yanru Huang, Xingmei Yao, Lutan Zhang, Yixi Zhou, Wenbo Wang, Jian Zhang, Yunsheng Ge   +7 more
wiley   +1 more source

Effect of aging on the configurational change of the aortic arch

Geriatric Care, 2016
We explored the relationship between aging and the configuration of the aortic arch using computed tomography angiography (CTA). We retrospectively reviewed CTA obtained in 140 cases.
Atsuhiro Kojima, Isako Saga
doaj   +1 more source

Prediction of coarctation of the aorta in fetuses with transposition of great arteries: Inverted ventricular discrepancy as a predictor of arch repair in TGA. [PDF]

Acta Obstet Gynecol Scand
Fetal MV/TV ratio offers a simple and reproducible marker of AAO in TGA with a cutoff of ≥ 1.0 accurately predicting the need for arch repair. This simple echocardiographic marker improves prenatal risk stratification and surgical planning, facilitating prenatal counseling. Abstract Introduction Transposition of great arteries (TGA) with coarctation of
Campanale CM, Moras P, Ventrella S, Masci M, Pasquini L, Toscano A.   +5 more
europepmc   +2 more sources