Results 41 to 50 of about 11,540 (186)

Successful Management in an Infant Patient of PHACE Syndrome with a Complicated Aortic Arch Anomaly

Case Reports in Pediatrics, 2022
PHACE syndrome is a congenital disorder often associated with a cervicofacial infantile hemangioma and complicated cardiovascular malformations. Patients with PHACE syndrome often have complex aortic arch anomalies, longer aortic stenosis or agenesis ...
Shun Suzuki, Mitsuru Seki, Koichi Kataoka, Reina Koga, Tomoyuki Sato, Masaaki Kawada, Takanori Yamagata   +6 more
doaj   +1 more source

Structural Covariance Analysis of Altered Brain Development in Neonates With Congenital Heart Disease After Surgery

Journal of Magnetic Resonance Imaging, EarlyView.
ABSTRACT Background Brain development is altered in neonates with congenital heart disease (CHD), with well‐characterised reductions in regional brain volumes and enlargement of CSF spaces. However, perioperative morphological changes remain incompletely understood. Purpose To identify brain regions showing spatial patterns of coordinated expansion and
Mirthe E. M. van der Meijden, Barat Gal‐Er, Benjamin Clayden, Siân Wilson, Daniel Cromb, Andrew T. M. Chew, Alexia Egloff, Kuberan Pushparajah, John Simpson, Joseph V. Hajnal, A. David Edwards, Mary Rutherford, Jonathan O'Muircheartaigh, Serena J. Counsell, Alexandra F. Bonthrone   +14 more
wiley   +1 more source

Diagnostic Yield of Post‐Mortem Fetal Micro‐CT for Thoracic Abnormalities

Prenatal Diagnosis, EarlyView.
ABSTRACT Objective This study aims to identify the imaging findings specifically for thoracic anomalies in 1200 Micro‐CT cases, independent of whether the abnormality contributed to the main diagnosis or cause of death. Method We analyzed 1200 Micro‐CT scans in an unselected, consecutive cohort between 2017 and 2024 to identify thoracic anomalies ...
Ian C. Simcock, Audrey Lamouroux, Susan C. Shelmerdine, J. Ciaran Hutchinson, Neil J. Sebire, Owen J. Arthurs   +5 more
wiley   +1 more source

Transplacental Flecainide and/or Digoxin for Fetal Tachyarrhythmias: Therapeutic Efficacy and Clinical Experience

Prenatal Diagnosis, EarlyView.
ABSTRACT Objective To assess the efficacy and safety of transplacental flecainide and/or digoxin for fetal tachyarrhythmias when sotalol is unavailable. Method We evaluated transplacental flecainide, digoxin, or combination therapy in a retrospective and prospective cohort across two Thai tertiary centers.
Mukpradab Darakamas, Sanitra Anuwutnavin, Fuanglada Tongprasert, Wisit Chankhunaphas, Kanyarat Nilto, Supaluck Kanjanauthai, Jarupim Soongswang   +6 more
wiley   +1 more source

Congenital arch vessel anomalies in CHARGE syndrome: A frequent feature with risk for co-morbidity

International Journal of Cardiology: Heart & Vasculature, 2016
Background: CHARGE syndrome is a complex multiple congenital malformation disorder with variable expression that is caused by mutations in the CHD7 gene.
Nicole Corsten-Janssen, Conny M.A. van Ravenswaaij-Arts, Livia Kapusta   +2 more
doaj   +1 more source

Prenatal imaging phenotypes and outcomes of umbilical‐portal‐systemic venous shunts in singleton and twin pregnancies: A historical cohort study

Acta Obstetricia et Gynecologica Scandinavica, EarlyView.
This retrospective cohort compared umbilical‐portal‐systemic venous shunts in singleton and twin pregnancies. Type III was the most common subtype in singletons, whereas Type II was the most common in twins. Fetal growth restriction was more frequent in twins, but primary structural anomaly rates were similar.
Yun Zhang, Meng Meng, Fengyu Wu, Jianping Chen, Fenhe Zhou, Yuchun Ge, Ya Xing, Xinyao Zhou, Gang Zou   +8 more
wiley   +1 more source

Multiscale Modeling of a Geometrically Tunable Shunt for Growing Pediatric Patients With Single Ventricle Physiology

Artificial Organs, EarlyView.
Here we investigated the development of a geometrically tunable blood for patients with single ventricle physiology. Two multiscale cardiovascular models were customized and implemented at timepoints spanning across the beginning and end of the shunt‐use period.
Ellen E. Garven, Ethan Kung, Randy M. Stevens, Christopher B. Rodell, Amy L. Throckmorton   +4 more
wiley   +1 more source

Expanding the Phenotypic Spectrum of FTO‐Related Developmental Disorder Caused by Biallelic Variants in FTO

Clinical Genetics, EarlyView.
We report 13 additional individuals from nine families, evaluating in detail the genotypic and phenotypic spectrum in comparison with the previously reported individuals. Our work substantially broadens the phenotypic spectrum, ranging from the severe and lethal to a milder developmental phenotype.
Radhakrishnan Periyasamy, Gopika Kanippayyur Narayanan, Dhanya Lakshmi Narayanan, Nisha Mohan, Sheela Nampoothiri, Dhanya Yesodharan, Mathilde Nizon, Leïla Ghesh, Meenakshi Bhat, Monisha Morris, Sarah Ghazali, Mahmoud Almutadares, Deema Aljeaid, Shahyan Siddiqui, Anju Shukla, Isabel Filges   +15 more
wiley   +1 more source

Cerebral Ventriculomegaly With Abnormality of the Aqueduct of Sylvius: A Case Series

Clinical Genetics, EarlyView.
Genetic testing leads to a diagnostic rate of ~30% in a fetal cohort with cerebral ventriculomegaly where the neuropathological examination revealed a stenosis or atresia of the aqueduct of Sylvius. ABSTRACT Fetal cerebral ventriculomegalies are brain anomalies with potentially poor neurodevelopmental prognosis.
Romain Nicolle, Laurence Loeuillet, Bettina Bessieres, Lucile Boutaud, Sarah Grotto, Nicolas Bourgon, Maryse Bonniere, Jelena Martinovic, Aude Tessier, Nathalie Roux, Giulia Petrilli, Naima Talhi, Marion Lesieur‐Sebellin, Jérémy Bertrand, Anaïs L'haridon, Aurélie Coussement, Marie‐Laure Maurin, Marie‐Paule Beaujard, Valérie Malan, Férechté Razavi, Tania Attie‐Bitach   +20 more
wiley   +1 more source

Isolation of Left Common Carotid Artery with Its Origin Proximal to Patent Ductus Arteriosus Presenting in Adult Age

Case Reports in Radiology, 2016
Anomalies of aortic arch are a common occurrence. Such anomalies of right sided aortic arch with its various branching patterns are of clinical importance.
Anagha R. Joshi, Saurabh Joshi, Kiran Kale, Rahul Jain, Jernail Singh Bava   +4 more
doaj   +1 more source