Results 31 to 40 of about 2,415 (196)

Outcome of prenatally diagnosed fetal heterotaxy: A systematic review and meta-analysis. [PDF]

, 2017
OBJECTIVES: To assess the perinatal outcomes of fetuses affected by heterotaxy. METHODS: Medline, Embase and Cinhal were searched. Only studies reporting a prenatal diagnosis of isomerism were included.
Abuhamad, Atkinson, Bardin, Baschat, Berg, Bronshtein, Brueckner, Carvalho, Collins, Degenhardt, Ditchfield, Dreux, Egger, Escobar-Diaz, Friedberg, Gaur, Gottschalk, Henderson, Ho, Hoefstaetter, Hunter, Icardo, Jacobs, Kennedy, Kheiri, Kothari, Ladd, Lee, Leeflang, Lim, Lin, Loomba, Loomba, Manzoli, McKiernan, Nakada, Nemec, NHS Centre for Reviews and Dissemination, Ozkutlu, Paladini, Pasquini, Peoples, Pepes, Phoon, Pockett, Shen, Shen, Taketazu, Tan, Tan, Varela-Fascinetto, Yan   +51 more
core   +1 more source

Heterotaxia associated with polysplenia [PDF]

BMJ Case Reports, 2014
A 31-year-old man underwent abdominal CT for blunt abdominal trauma. CT scan demonstrated cardiac apex (figure 1A), stomach (figure 1B, C) and multiple splenic nodules situated on the left of the midsagittal plane; liver and inferior vena cava on the right and abdominal aorta in the midline (figure 1B–D).
Idil Gunes, Tatar, Onur, Ergun, Hale, Altunoglu, Tolga, Tatar   +3 more
openaire   +2 more sources

Heterotaxy pattern associated with sinus node dysfunction in an adult: A case report

Clinical Case Reports, 2023
Key Clinical Message A 26‐year‐old male patient admitted to the hospital ward with experience of repetitive syncopes for a year. The patient was diagnosed with sick sinus syndrome.
Naman Shah, Sankalp Acharya, Apoorva Tripathi, Himanshi Bisht, Maitri Shah, Aayushi Pareek, Asmita Gera, Abhigan Babu Shrestha, Vikash Jaiswal   +8 more
doaj   +1 more source

Heart transplantation in children with congenital heart disease [PDF]

, 1932
ObjectivesThe aim of this study was to describe heart transplantation in children with congenital heart disease and to compare the results with those in children undergoing transplantation for other cardiac diseases.BackgroundReports describe decreased ...
Daphne T. Hsu, Jan M. Quaegebeur, Robert E. Michler, Craig R. Smith, Eric A. Rose, Maryanne R. Kichuk, Welton M. Gersony, Judith F. Douglas, Linda J. Addonizio, Morris, Fontan, Hosenpud, Doty, Chartrand, Mayer, Cooper, Bailey, Menkis, Richenbacher, Harjula, Rietz, Radley-Smith, Trento, Armitage, Hasan, Addonizio, Chartrand, Baum, Merrill, Addonizio, Triedman   +30 more
core   +1 more source

Risk factors for Fontan-associated hepatocellular carcinoma.

PLoS ONE, 2022
AimsThe incidence of hepatocellular carcinoma (HCC) in patients with Fontan-associated liver disease (i.e., FALD-HCC) has increased over time. However, the risk factors for HCC development remain unclear.
Tomomi Kogiso, Takaomi Sagawa, Makiko Taniai, Eriko Shimada, Kei Inai, Tokuko Shinohara, Katsutoshi Tokushige   +6 more
doaj   +1 more source

Extrahepatic Anomalies in Infants With Biliary Atresia: Results of a Large Prospective North American Multicenter Study [PDF]

, 2013
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/100275/1/hep26512 ...
Bezerra, Jorge A, Bove, Kevin, Haber, Barbara H, Karpen, Saul J, Kerkar, Nanda, Mack, Cara L, Magee, John C, Molleston, Jean P, Moore, Jeffrey, Murray, Karen F, Network, Childhood Liver Disease Research and Education, Ng, Vicky L, Romero, René, Rosenthal, Philip, Schwarz, Kathleen B, Shneider, Benjamin L, Sokol, Ronald J, Turmelle, Yumirle P, Wang, Kasper S, Whitington, Peter F   +19 more
core   +2 more sources

Left ventricular hypertrabeculation/noncompaction with epilepsy, other heart defects, minor facial anomalies and new copy number variants [PDF]

, 2012
BACKGROUND: Left ventricular hypertrabeculation/noncompaction (LVHT) is a cardiac abnormality of unknown etiology which has been described in children as well as in adults with and without chromosomal aberrations.
Bert Nagel, Claudia Stöllberger, Eva Klopocki, Josef Finsterer, Sabine Uhrig, Ursula Gruber-Sedlmayr   +5 more
core   +1 more source

A 0.5-Mbp deletion on bovine chromosome 23 is a strong candidate for stillbirth in Nordic Red cattle [PDF]

, 2016
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de Koning, Dirk-Jan, Guldbrandtsen, Bernt, Iso-Touru, Terhi, Sahana, Goutam, Sander Nielsen, Ulrik, Sandø Lund, Mogens, Vilkki, Johanna, Wu, Xiaoping   +7 more
core   +7 more sources

Thoracoscopic oesophago-oesophagostomy in the prone position for oesophageal stenosis caused by dilated azygos vein in polysplenia-associated heterotaxy

Journal of Minimal Access Surgery, 2021
Background: Heterotaxy syndrome is associated with a plethora of cardiovascular and other multi-system anomalies with a high childhood mortality. A dilated azygos vein as part of the polysplenia variant of heterotaxy syndrome may cause oesophageal ...
Rajesh Bhojwani, Nikhil Jain
doaj   +1 more source

Mild fetal cerebral ventriculomegaly as a prenatal sonographic marker for Kartagener syndrome [PDF]

, 2003
Primary ciliary dyskinesia (PCD), also referred to as immotile-cilia syndrome or Kartagener syndrome, is a group of genetic disorders caused by defective cilia leading to chronic sinupulmonary infection, situs inversus and reduced fertility.
Afzelius, Afzelius, Bloom, Bromley, Brueckner, Bryan, Chen, Daniel, De Santi, Dhein, Edwards, Greenstone, Guichard, Hackett, Ibañez-Tallon, Jabourian, Kelly, Losa, Mercier, Monnet, Nakamura, Nonaka, Olbrich, Pennarun, Picco, Pilu, Shimizu, Torikata, Vergani, Whitelaw   +29 more
core   +1 more source