Results 141 to 150 of about 2,246,280 (273)

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

Commentary: ‘Which outcome for patients with functional single ventricles and heterotaxy syndrome?’ [PDF]

, 2023
Gianluigi Perri, Victoria D’Inzeo, Lorenzo Galletti   +2 more
openalex   +1 more source

Sleep and Rhythmic Profile After Pineal Gland Removal in Humans

Journal of Sleep Research, EarlyView.
ABSTRACT Melatonin, a hormone produced by the pineal gland, is classically described as a central circadian modulator. However, the impact of its absence on circadian rhythmicity in humans remains poorly understood. Pinealectomised patients, in whom melatonin secretion is chronically suppressed, represent a valuable clinical model to investigate the ...
Renata de Andrade Prado Gobetti, Clarissa Bueno, Letícia M. S. F. A. Soster, Anna Carolina de Campos de Barros Luvizotto Monazzi, Fernanda Gaspar do Amaral, Andréa Maria Capellano, Nasjla Saba da Silva, José Cipolla‐Neto   +7 more
wiley   +1 more source

Peritoneal metastatic adenocarcinoma possibly due to a gastric duplication cyst: a case report and literature review [PDF]

, 2014
BACKGROUND: Gastric duplication cysts are rare congenital abnormalities, and malignant transformation of these duplications is also thought to be rare. CASE PRESENTATION: During a routine health checkup, a 28-year-old man underwent abdominal sonography ...
Hong Chang, Hong Liu, Hui Su, Jing Wu, Kuiliang Liu, Mingming Meng, Weiping Tai, Xiangchun Lin   +7 more
core   +1 more source

Role of spin echo and cine magnetic resonance imaging in presurgical planning of heterotaxy syndrome. Comparison with echocardiography and catheterization. [PDF]

, 1994
Tal Geva, G. Wesley Vick, Richard E. Wendt, Roxann Rokey   +3 more
openalex   +1 more source

Delayed Dental Development in Children With Non‐Syndromic Hypodontia: A Cross‐Sectional Study Using a Machine Learning Approach to Dental Age Estimation

Orthodontics &Craniofacial Research, EarlyView.
ABSTRACT Objectives To investigate the influence of non‐syndromic hypodontia on radiographic dental development and to estimate dental age in children with bilateral mandibular agenesis using a machine learning approach. Materials and Methods This retrospective cross‐sectional study included 626 children aged 6–15 years (311 with dental agenesis, 315 ...
Marine Crosnier, Pierre‐Hadrien Decaup, Frédéric Santos, Anaïs Cavare   +3 more
wiley   +1 more source

Coexistence of coloboma, heart defects, atresia choanae, growth retardation, genital abnormalities, and ear anomalies (CHARGE) syndrome and heterotaxy in a newborn with athymia

Journal of Allergy and Clinical Immunology: Global
The case presented highlights a unique presentation of coloboma, heart defects, atresia choanae, growth retardation, genital abnormalities, and ear anomalies (CHARGE) syndrome along with athymia and heterotaxy to establish a possible association between ...
Rica Patil, DO, Jacquelyn Hunter, MD, Alan Knutsen, MD, Stephen R. Braddock, MD   +3 more
doaj   +1 more source

Indications for cardiovascular magnetic resonance in children with congenital and acquired heart disease: an expert consensus paper of the Imaging Working Group of the AEPC and the Cardiovascular Magnetic Resonance Section of the EACVI [PDF]

, 2017
This article provides expert opinion on the use of cardiovascular magnetic resonance (CMR) in young patients with congenital heart disease (CHD) and in specific clinical situations. As peculiar challenges apply to imaging children, paediatric aspects are
Beerbaum, P., Bonello, B., Brockmeier, Konrad, Brockmeier, Konrad, Bucciarelli-Ducci, C., Edvardsen, Thor, Edvardsen, Thor, Eichhorn, J., Fratz, S., Galderisi, Maurizio, Galderisi, Maurizio, Greil, G.F., Grosse-Wortmann, L., Helbing, W.A., Miller, Owen, Miller, Owen, Qureshi, Shakeel, Qureshi, Shakeel, Sarikouch, S., Schwitter, J., Sicari, Rosa, Sicari, Rosa, Sieverding, L., Simpson, John, Simpson, John, Stein, Joerg, Stein, Joerg, Thaulow, Erik, Thaulow, Erik, Valsangiacomo Buechel, E.R.   +29 more
core  

The Current Landscape of Genetic Testing in Cardiovascular Malformations: Opportunities and Challenges [PDF]

, 2016
Human cardiovascular malformations (CVMs) frequently have a genetic contribution. Through the application of novel technologies, such as next-generation sequencing, DNA sequence variants associated with CVMs are being identified at a rapid pace.
Landis, Benjamin J., Ware, Stephanie M.
core   +2 more sources

Genetic Diagnoses Among Congenital Anomaly Cases in Europe: Data From the EUROCAT Network

Paediatric and Perinatal Epidemiology, EarlyView.
ABSTRACT Background Surveillance of congenital anomaly prevalence over time can identify new teratogens. Anomalies with a genetic cause are excluded from the monitoring. Objectives We examined temporal changes in the proportion of genetic diagnoses among cases with a congenital anomaly.
Jorieke E. H. Bergman, Annie Perraud, Ester Garne, Ingeborg Barisic, David Tucker, Elisa Ballardini, Lea Bruneau, Clara Cavero‐Carbonell, Ianis Cousin, Miriam Gatt, Katya Kovacheva, Anna Latos‐Bielenska, Mary O'Mahony, Isabelle Monier, Isabelle Perthus, Riccardo Pertile, Anke Rissmann, Florence Rouget, Michelle Santoro, Joanna Sichitiu, Christine Verellen‐Dumoulin, Wladimir Wertelecki, Diana Wellesley, Joan K. Morris   +23 more
wiley   +1 more source