Results 141 to 150 of about 3,631,363 (269)

Pilot study exploring artificial intelligence for facial-image-based diagnosis of Marfan syndrome

Heliyon
Background: Marfan Syndrome (MFS), a genetic disorder impacting connective tissue, manifests in a wide array of phenotypes which can affect numerous bodily systems, especially the thoracic aorta.
Danny Saksenberg, Sandip Mukherjee, Mohammad A. Zafar, Bulat Ziganshin, John A. Elefteriades   +4 more
doaj   +1 more source

Aortic aneurysm and non-Hodgkin’s lymphoma in Marfan syndrome

Turkish Journal of Hematology, 2009
The combination of Marfan syndrome with lymphoma is extremely rare. This report describes a case of Marfan syndrome who presented with chest discomfort and was diagnosed to have an aortic aneurysm and an additional incidental mediastinal mass that on ...
Sujoy Ghosh, Subrata Ghosh, Sandip Kumar Ghosh   +2 more
doaj  

Lebensqualität herzoperierter und nicht herzoperierter Marfan-Patienten in der Schweiz

, 2008
Ein Handbuch für Betroffene seltener Krankheiten und ihr Umfeld. Das Bewältigen einer chronischen Krankheit stellt an die betroffenen Menschen hohe Anforderungen. Erst recht, wenn die Krankheit selten ist. Wie gehen sie damit um? Welche Unterstützung
Carrel, T, Carrel, Thierry, Steinmann, B, Immer, Franz, Steinmann, Beat, Marti, P, Immer, F, Marti, Philippe   +7 more
core  

Marfan′s syndrome

Heart Views, 2012
Tanuj Bhatia, Aditya Kapoor, Sudeep Kumar   +2 more
openaire   +3 more sources

Cecal volvulus in Marfan Syndrome [PDF]

Gastrointestinal pathology in adult patients with Marfan Syndrome is rarely reported in literature. Nevertheless, it could be life threatening when it occurs.
Rashid, Amir, Ward, Stephen, Yip, Swee Yan   +2 more
core   +1 more source

Altered Gait Mechanics in Marfan Syndrome

FBN1 is a gene responsible for the production of fibrillin, a major component of connective tissue throughout the body including skeletal muscle tissue. In individuals with Marfan Syndrome these mutations in FBN1 result in widespread muscle weakness and ...
Sharp, Amara G
core   +1 more source

Is Marfan Syndrome Associated With Symptomatic Intracranial Aneurysms?

, 1996
Background and Purpose Marfan syndrome is a heritable disorder of connective tissue caused by a deficiency of the glycoprotein fibrillin.
M. Limburg, R.C.M. Hennekam, J.S.P. van den Berg   +2 more
core   +1 more source

Case Report: A rare coexistence with severe aortic root dilatation and nutcracker phenomenon in pediatric Marfan syndrome

Frontiers in Pediatrics
Marfan syndrome (MFS) is a multisystem connective tissue disorder affecting the cardiovascular, ocular, and skeletal systems. We report a case of a 13.5-year-old boy who presented with excessive linear growth.
Xiaoyu Qiao, Xiaoyu Qiao, Xiaoyu Qiao, Xiaoyu Qiao, Yanyu Chen, Yanyu Chen, Danyan Su, Danyan Su, Lifeng Shang, Lifeng Shang, Yusheng Pang, Yusheng Pang   +11 more
doaj   +1 more source

The revised Ghent nosology for the Marfan syndrome

Journal of Medical Genetics, 2010
B. Loeys, H. Dietz, A. Braverman, B. Callewaert, J. D. De Backer, R. Devereux, Y. Hilhorst-Hofstee, G. Jondeau, L. Faivre, D. Milewicz, R. Pyeritz, P. Sponseller, Paul Wordsworth, A. De Paepe   +13 more
semanticscholar   +1 more source

AN EXCLUSION MAP OF MARFAN-SYNDROME

, 1990
The combined genetic data between the Marfan syndrome and 75 informative loci on 18 autosomes were used to construct an exclusion map for this disorder. Data are also presented for a further two unmapped markers.
Blanton, S H, Farndon, PA, Sarfarazi, M, Kilpatrick, M W, Blanton, SH, Child, AH, Child, A H, Pope, F M, Eiberg, H, de Groote, J, Francomano, CA, Peltonen, L, Kilpatrick, MW, Farndon, P A, Pope, FM, Francomano, C A, J de Groote, H Eiberg, F M Pope, A H Child, M W Kilpatrick, L Peltonen, M Sarfarazi, S H Blanton, C A Francomano, P A Farndon   +25 more
core   +1 more source