Results 71 to 80 of about 2,459 (211)

CHD associated with syndromic diagnoses: peri-operative risk factors and early outcomes [PDF]

, 2015
CHD is frequently associated with a genetic syndrome. These syndromes often present specific cardiovascular and non-cardiovascular co-morbidities that confer significant peri-operative risks affecting multiple organ systems.
Cooper, David S., Hinton, Robert B., Landis, Benjamin J.   +2 more
core   +1 more source

Vitamin K deficiency bleeding and optimal prophylaxis methods in biliary atresia: A surveillance study in Japan

Pediatrics International, Volume 67, Issue 1, January/December 2025.
Abstract Background Vitamin K (VK) prophylaxis refers to the administration of VK to newborns to prevent neonatal VK deficiency bleeding (VKDB), which is characterized by intracranial hemorrhage (ICH). This study investigated the relationship between VK prophylaxis methods and VKDB in biliary atresia (BA).
Ryuji Okubo, Chiyoe Shirota, Motoshi Wada, Masato Shinkai, Hirofumi Tomita, Satoshi Umeda, Hiromu Miyake, Toshiharu Matsuura, Shigehisa Fumino, Akio Odaka, Taizo Hibi, Toshio Harumatsu, Akiko Yokoi, Tomoro Hishiki, Shigeru Ono, Kohei Matsushita, the Japanese Biliary Atresia Society   +16 more
wiley   +1 more source

Polüspleeniaga heterotaksia sündroom [PDF]

, 2015
Eesti Arst 2015; 94(11):675 ...
Tiivel, Marek
core   +2 more sources

Long‐Read Sequencing as a Diagnostic Tool for Primary Ciliary Dyskinesia

Case Reports in Genetics, Volume 2025, Issue 1, 2025.
Primary ciliary dyskinesia (PCD) is a rare, inherited disease resulting from abnormal structure and/or function of cilia. To date, pathogenic variants in over 50 genes have been reported as causes of PCD. One of the genes, HYDIN, presents a diagnostic challenge due to the existence of HYDIN2, a highly homologous pseudogene that significantly ...
Liora H. Feshbach, Morgan Similuk, Laura M. Amendola, Katie L. Lewis, Magdalena A. Walkiewicz, Mari Tokita, Rajarshi Ghosh, Andrew Lipton, Balraj Mittal   +8 more
wiley   +1 more source

Left atrial isomerism associated with aneurysmal enlargement of right atrial appendage: A case report with literature review

Indian Journal of Radiology and Imaging, 2019
We present a prenatally diagnosed case of heterotaxy syndrome (HS) in which left atrial isomerism (LAI) was associated with an aneurysmal enlargement of the right atrial appendage (RAA).
Prateek Agarwal, Rajesh Kumar Agarwal
doaj   +1 more source

Splenic duplication: a rare cause of acute upper gastrointestinal bleeding [PDF]

, 2018
Acute gastrointestinal bleeding represents a common medical emergency. We report the rare case of acute upper gastrointestinal bleeding caused by varices in the gastric fundus secondary to splenic duplication.
Alkadhi, Hatem, Bauerfeind, Peter, Gubler, Christoph, Pfammatter, Thomas, Sharma, Pankaj   +4 more
core  

Fetal Presentation of MYRF‐Related Cardiac Urogenital Syndrome: An Emerging and Challenging Prenatal Diagnosis

Prenatal Diagnosis, Volume 44, Issue 13, Page 1647-1658, December 2024.
ABSTRACT Purpose MYRF‐related cardiac‐urogenital syndrome (MYRF‐CUGS) is a rare condition associated with heterozygous MYRF variants. The description of MYRF‐CUGS phenotype is mostly based on postnatal cases and 36 affected individuals have been published so far.
Maud Favier, Elise Brischoux‐Boucher, Louise C. Pyle, Nicolas Mottet, Marion Auber‐Lenoir, Julie Cattin, Eric Dahlen, Christelle Cabrol, Francine Arbez‐Gindre, Tania Attié‐Bitach, Odile Boute, Louise Devisme, Detlef Trost, Aicha Boughalem, David Chitayat, Lev Prasov, Odelia Chorin, Annick Rein‐Rothschild, Eran Kassif, Tal Weissbach, Laura Godfrey Hendon, Margaret P. Adam, Chloé Quelin, Sylvie Jaillard, Laura Mary, Sietse M. Aukema, Malou Heijligers, Christine de Die‐Smulders, Sander Stegmann, Lauren Badalato, Adi Ben‐Yehuda, Claire Beneteau, Pierre‐Louis Forey, Paul Kuentz, Juliette Piard   +34 more
wiley   +1 more source

Polysplenia Syndrome With Persistent Left Superior Vena Cava: Case Report and Review of the Literature

Global Pediatric Health, 2022
Polysplenia syndrome is an uncommon condition associating several splenic nodules (sometimes polylobed spleen and cases of normal spleen have been described) with a number of malformations that appear between the fourth and sixth week of embryonic ...
El Houss Salma MD, Amsiguine Najwa MD, Tantaoui Mehdi MD, Allali Nazik PhD, Chat Latifa PhD, El Haddad Siham PhD   +5 more
doaj   +1 more source

Retrospective Cohort Study of Associated Factors for Intestinal Complications in Pediatric Liver Transplantation

Pediatric Transplantation, Volume 28, Issue 8, December 2024.
Intestinal complications (IC) are significant adverse events following liver transplantation (LT), yet research on pediatric cohorts remains limited. This study aims to describe IC in children after LT and identify factors associated with their occurrence.
Sindy Pires, Valérie A. McLin, Nathalie Rock, Ana‐Maria Calinescu, Barbara E. Wildhaber   +4 more
wiley   +1 more source

Introduction of transcatheter edge‐to‐edge repair in patients with congenital heart disease at a children's hospital

Catheterization and Cardiovascular Interventions, Volume 103, Issue 2, Page 326-334, February 1, 2024.
Abstract Background Atrioventricular valve regurgitation (AVVR) is a devastating complication in children and young adults with congenital heart disease (CHD), particularly in patients with single ventricle physiology. Transcatheter edge‐to‐edge repair (TEER) is a rapidly expanding, minimally invasive option for the treatment of AVVR in adults that ...
Matthew A. Jolley, Analise Sulentic, Silvani Amin, Mudit Gupta, Stephen Ching, Alana Cianciulli, Yan Wang, Patricia Sabin, Christopher Zelonis, Matthew Daemer, Elizabeth Silvestro, Keith Coleman, Lauren K. Ford, Jonathan B. Edelson, Emily S. Ruckdeschel, Meryl S. Cohen, Susan C. Nicolson, Matthew J. Gillespie   +17 more
wiley   +1 more source