Results 31 to 40 of about 4,442 (232)

Syndrome of right isomerism: Ivemark syndrome

Journal of Mahatma Gandhi Institute of Medical Sciences, 2018
Heterotaxy Syndrome is a complex syndrome that occurs when the axes of the body fail to rotate correctly when developing in the uterus. This can result in many different organ systems being affected.
Dipti Jain, Bhushan Chavan, Anita Manoj
doaj   +1 more source

Heterotaxy syndrome with left atrial isomerism and polysplenia is a unique entity: a case report

Egyptian Journal of Chest Disease and Tuberculosis, 2021
A state of a patient with heterotaxy syndrome with polysplenia was indiscriminately diagnosed through visualized estimation (computed tomography and pelviabdominal ultrasound) regardless of the pathological state.
Rana El-Helbawy, Ibrahim Elmahalawy, Mohammed A Agha   +2 more
doaj   +1 more source

Heterotaxy Polysplenia Syndrome Causing Intermittent Vomiting Due to Malrotation of the Duodenum in an Adult

Haseki Tıp Bülteni, 2019
Heterotaxy syndrome (situs ambiguus) is a rare condition in which the internal organs are abnormally arranged in the chest and abdomen. It occurs from an early embryological developmental disturbance with most cases being sporadic.
Tuba Selçuk Can, Behice Kaniye Yılmaz, Yıldıray Savaş   +2 more
doaj   +1 more source

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

A Rare Variation of the Heterotaxy Syndrome

Case Reports in Medicine, 2012
Heterotaxy syndrome is a rare, complex, and confusing type of the situs anomalies. It is not possible to estimate the degree of lateralization, isomerism, and rotational variation in these types of cases.
Alper Dilli, Salih Sinan Gultekin, Umit Yasar Ayaz, Hatice Kaplanoglu, Baki Hekimoglu   +4 more
doaj   +1 more source

Antenatal diagnosis of left atrial isomerism and heterotaxy syndrome in fetus with Meckel-Gruber syndrome

Türk Kardiyoloji Derneği Arşivi, 2014
We aimed to present a fetus with Meckel-Gruber syndrome (MKS) who had left atrial isomerism, heterotaxy syndrome and complete heart block. A 26-year-old healthy female was referred to our clinic in the 23rd week of her pregnancy.
Seçil Kurtulmuş, Savaş Demirpençe, Deniz Can Öztekin, Altuğ Koç, Vedide Tavlı   +4 more
doaj   +1 more source

3D printing is a transformative technology in congenital heart disease [PDF]

, 2018
Survival in congenital heart disease has steadily improved since 1938, when Dr. Robert Gross successfully ligated for the first time a patent ductus arteriosus in a 7-year-old child.
Anwar, Anwar, Barach, Bernhard, Bhatla, Biglino, Biglino, Binder, Boneva, Borrello, Botto, Brown, Bucher, Byrne, Chaowu, Conti, Costello, Dearani, Deferm, Duan, Duan, Erikssen, Fan, Farooqi, Farooqi, Farooqi, Fleming, Fukunishi, Garekar, Gaynor, Gentles, Giamberti, Giannopoulos, Giroud, Gosnell, Grant, Green, Hadeed, Hermsen, Hoffman, Holst, Holst, Hu, Jacobs, Jana, Javan, Jonas, Kappetein, Kapur, Khairy, Kiraly, Kirklin, Kolli, Kotsis, Kung, Lee, Lee, Little, Lloyd-Jones, Mahle, Mahmood, Mannoor, Maragiannis, Markert, Markstedt, Mashari, Meier, Michael, Mitsouras, Moons, Moore, Morrison, Muraru, Ngan, Noecker, Olivieri, Olivieri, O’Brien, O’Neill, Pentecost, Poterucha, Randazzo, Rehder, Riesenkampff, Ripley, Rodriguez-Paz, Ryan, Saeed, Samuel, Santos dos, Schievano, Schmauss, Shah, Smith, Sodian, Sodian, Sutcliffe, Tabriz, Tack, Taylor, Valverde, VanKoevering, Vukicevic, Vukicevic, Vukicevic, Wang, Wang, Warnes, Warnes, Warnes, Whitlock, Wilasrusmee, Williams, Witschey, Yoo, Yoo, Zopf, Zweifel   +117 more
core   +3 more sources

Systems Analysis Implicates WAVE2 Complex in the Pathogenesis of Developmental Left-Sided Obstructive Heart Defects. [PDF]

, 2020
Genetic variants are the primary driver of congenital heart disease (CHD) pathogenesis. However, our ability to identify causative variants is limited.
Bernstein, Daniel, Bisgrove, Brent W, Brueckner, Martina, Chung, Wendy K, Deanfield, John, Demarest, Bradley, Edwards, Jonathan J, Fernandez, Nicolas F, Gelb, Bruce D, Giardini, Alessandro, Goldmuntz, Elizabeth, Kim, Richard, Lachmann, Alexander, Lifton, Richard P, Ma'ayan, Avi, Newburger, Jane W, Porter, George, Roberts, Amy E, Rouillard, Andrew D, Seidman, Christine E, Shankaran, Sunita S, Srivastava, Deepak, Tristani-Firouzi, Martin, Turan, Nahid, Wang, Zichen, Yost, H Joseph   +25 more
core  

The analysis of heterotaxy patients reveals new loss-of-function variants of GRK5 [PDF]

, 2016
G protein-coupled receptor kinase 5 (GRK5) is a regulator of cardiac performance and a potential therapeutic target in heart failure in the adult. Additionally, we have previously classified GRK5 as a determinant of left-right asymmetry and proper heart ...
Bauer, Ulrike M. M., Burkhalter, Martin D., Hitz, Marc-Phillip, Kubisch, Christian, Lessel, Davor, Moepps, Barbara, Muhammad, Tariq, Philipp, Melanie, Rentzsch, Axel, Schalinski, Adelheid, Schubert, Stephan, Tena, Teresa Casar, Toka, Okan, Ware, Stephanie M.   +13 more
core   +2 more sources

Heterotaxy Syndrome and Spectrum of Cardiac Involvement

Journal of the Indian Academy of Echocardiography & Cardiovascular Imaging
Heterotaxy syndrome, a birth defect characterized by abnormal arrangement of organs, is strongly associated with complex congenital heart disease (CHD).
Munesh Tomar, Maitri Chaudhuri
doaj   +1 more source