Results 121 to 130 of about 1,256,915 (264)

Successful heart transplantation in a patient with Ivemark syndrome combined with situs inversus, single atrium and ventricle after total cavo-pulmonary connection [PDF]

, 2017
Heart transplantation represents a valuable therapeutical option for patients with congenital heart disease and end-stage heart failure. We report the case of a young adult patient with a situs inversus and additional complex congenital malformations of ...
Althaus, Ulrich, Berdat, Pascal A., Carrel, Thierry, Mohacsi, Paul   +3 more
core  

Deranged Myocyte Microstructure in Situs Inversus Totalis Demonstrated by Diffusion Tensor Cardiac Magnetic Resonance.

JACC Cardiovascular Imaging, 2018
To the Editor: In situs inversus totalis (SIT), there is mirror imaging of the situs solitus (SS) visceral arrangement; however, there are no histological studies examining the myocardial microstructure.
Z. Khalique, P. Ferreira, A. Scott, S. Nielles-Vallespin, P. Kilner, R. Kutys, Maria E. Romero, A. Arai, D. Firmin, D. Pennell   +9 more
semanticscholar   +1 more source

Primary Ciliary Dyskinesia: An Update on Clinical Aspects, Genetics, Diagnosis, and Future Treatment Strategies [PDF]

, 2017
Primary ciliary dyskinesia (PCD) is an orphan disease (MIM 244400), autosomal recessive inherited, characterized by motile ciliary dysfunction. The estimated prevalence of PCD is 1:10,000 to 1:20,000 live-born children, but true prevalence could be even ...
Abete, Afzelius, Afzelius, Afzelius, Alanin, Altenburg, Bartoloni, Behan, Bhatt, Bilton, Boaretto, Boe, Boon, Boon, Boon, Bradley, Brenner, Brown, Bush, Bush, Campbell, Carotenuto, Chang, Chang, Chernick, Cohen-Cymberknoh, Cole, Coren, Davis, Daviskas, De Benedetti, Desai, Deuse, Eastham, El-Abiad, Eliasson, Elkins, Ellerman, Fedakar, Ferkol, Ferkol, Fliegauf, Fliegauf, Flume, Fokkens, Fretzayas, Frommer, Fuchs, Gokdemir, Goutaki, Halbert, Hart, Hellinckx, Hill, Horani, Horani, Irving, Jeanson, Kartagener, Kellett, Kennedy, Kennedy, Kennedy, Kim, King, Knowles, Knowles, Knowles, Kobbernagel, Konstan, Kott, Kuehni, Kumar, Lai, Lebl, Leigh, Lucas, Lucas, Lucas, Lucas, Macchiarini, Mackerness, Madsen, Maglione, Maglione, Manna, Marks, Marthin, Marthin, Marthin, Mateos-Corral, McManus, Merveille, Mirra, Mitchison, Montella, Montella, Montella, Montella, Moore, Mossberg, Mullowney, Munro, Nakhleh, Nicolson, Noone, Noone, Oktem, Olbrich, Omran, Onoufriadis, Onoufriadis, O’Callaghan, O’Callaghan, Paff, Paff, Papon, Pasteur, Patella, Phillips, Picot, Pifferi, Potter, Prulière-Escabasse, Raidt, Rogers, Rutland, Sagel, Santamaria, Santamaria, Schwabe, Serisier, Shah, Shapiro, Shoemark, Sommer, Spagnolo, Stenbit, Stillwell, Sturgess, Svobodova, ten Berge, Valerio, Walker, Wallmeier, Werner, Werner, Wirschell, Wong, Yan-Wei, Zimmerman   +150 more
core   +1 more source

Situs inversus totalis - a case report

National Journal of Clinical Anatomy, 2014
Situs inversus is a congenital positional anomaly characterized by transposition of abdominal viscera and when associated with right sided heart (Dextrocardia) is referred to as Situs inversus totalis.
Malamoni Dutta, Joydev Sarma
doaj   +1 more source

Kartagener Syndrome With Focal Segmental Glomerulosclerosis [PDF]

, 2013
Primary ciliary dyskinesia is characterized by congenital impairment of mucociliary clearance. Kartagener syndrome (KS) is a clinical variant of primary ciliary dyskinesia which is involved in situs inversus associated with chronic respiratory infections.
Doroushi, Behzad, Momeni, Ali, Taheri, Nadia   +2 more
core  

Functional modelling of a novel mutation in BBS5. [PDF]

, 2014
BACKGROUND: Bardet-Biedl syndrome (BBS) is an autosomal recessive ciliopathy disorder with 18 known causative genes (BBS1-18). The primary clinical features are renal abnormalities, rod-cone dystrophy, post-axial polydactyly, learning difficulties ...
Al-Fadhly, F., Al-Hamed, M.H., Chrystal, P., El Sayed, R., Eley, L., Hynes, A.M., Meyer, B., Sayer, J.A., Simms, R.J., van Lennep, C.   +9 more
core   +2 more sources

Kartagener’s Syndrome Presenting As Bilateral Recurrent Nasal Polyposis In A Young Boy

Journal of Bahria University Medical and Dental College, 2018
Kartagener's syndrome is a very rare congenital disease consists of a classic triad, sinusitis, situs inversus and bronchiectasis. Approximately one half of patients with primary ciliary dyskinesia have situs inversus and Kartagener syndrome.
Zeba Ahmed, Warda Waseem, Uroosa Saman
doaj   +1 more source

Case report about a successful full robotic radical gastric cancer surgery with intracorporeal robot-sewn anastomosis in a patient with situs inversus totalis and a two-and-a-half-year follow-up study

World Journal of Surgical Oncology, 2018
BackgroundDuring the last decade, total laparoscopic and laparoscopic-assisted distal gastrectomy for gastric cancer patients has been developed as alternatives to open resection.
Haifei Dai, Zhicheng Wang, Xiao-bo Feng, G. Wang, Wei-yan Li, C. Hang, Zhi-Wei Jiang   +6 more
semanticscholar   +1 more source

Situs inversus totalis with solid pseudopapillary pancreatic tumor

Medicine, 2018
Rationale: Situs inversus totalis (SIT) is a rare anatomical variation of the internal organs, and solid pseudopapillary tumor of the pancreas (SPTP) is a rare tissue type of pancreatic tumors, classified as benign or low-grade malignancy.
Deng Xiang, Jiannan He, Zimeng Fan, F. Xiong, Gang Liu, Sufen Chen, Wu Wen, Jianfeng Li, Junhua Ai, R. Wan, Gongxian Wang, Jun Shi   +11 more
semanticscholar   +1 more source

Echocardiographic recognition of a criss-cross heart with double outlet right ventricle [PDF]

, 2013
Crisscross heart (CCH) is a rare cardiac malformation characterized by crossing of the inflow streams of the two ventricles due to an apparent twisting of the heart about its long axis.
Taksande, Amar M.
core   +1 more source