Results 211 to 220 of about 3,631,363 (269)

Phenotypic Diversity of Marfan Syndrome. [PDF]

open access: yesJACC Adv
Xu Z   +11 more
europepmc   +1 more source

Marfan syndrome

open access: yesNursing
Abstract: This article provides a comprehensive review of Marfan Syndrome (MFS), covering its epidemiology, etiology, clinical presentations, diagnostics, complications, and treatment modalities. The Ghent II Nosology of MFS criteria are crucial in MFS diagnosis, guiding clinicians in identifying high-risk patients.
Petira, Filip
core   +5 more sources

Ocular manifestations of Marfan syndrome in children and adolescents

open access: yesEuropean Journal of Ophthalmology, 2019
Purpose: To study ocular manifestations of Marfan syndrome in children and adolescents. Methods: Retrospective comparative cohort study on consecutive patients up to age 17 years, presenting to the interdisciplinary Marfan clinic of Charité-University ...
D. Salchow, P. Gehle
semanticscholar   +2 more sources
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Marfan syndrome

Journal of the American Academy of Nurse Practitioners, 2009
AbstractPurpose: To provide an overview of Marfan syndrome (MFS), including diagnostic criteria, genetic factors involved, emerging theories for treatment, a case study, and an overview of genetic counseling for individuals and families of those with MFS.Data Sources: Selected research, review, and clinical articles.Conclusions: MFS is a connective ...
Eric D, Shirley, Paul D, Sponseller
openaire   +4 more sources

Perinatal diagnosis and management of early-onset Marfan syndrome: case report and systematic review

Journal of Maternal-Fetal & Neonatal Medicine, 2020
Early onset Marfan syndrome is the most severe form of Marfan syndrome diagnosed during perinatal period. Early onset Marfan syndrome is associated with high mortality rates, usually within the first 2 years of life.
A. Veiga-Fernández   +8 more
semanticscholar   +1 more source

Proximal aorta longitudinal strain predicts aortic root dilation rate and aortic events in Marfan syndrome.

European Heart Journal, 2019
AIMS Life expectancy in Marfan syndrome patients has improved thanks to the early detection of aortic dilation and prophylactic aortic root surgery.
A. Guala   +13 more
semanticscholar   +1 more source

Trends of vascular surgery procedures in Marfan syndrome and Ehlers-Danlos syndrome

Vascular, 2020
Objectives Marfan syndrome and Ehlers-Danlos syndrome represent two connective tissue vascular diseases requiring unique consideration in their vascular surgical care.
S. Jayarajan   +3 more
semanticscholar   +1 more source

Marfan's syndrome

American Heart Journal, 1953
Abstract A case of Marfan's syndrome exhibiting medial degeneration and aneurysmal formation with incomplete rupture of the pulmonary artery is reported with a review of the literature.
M, ANDERSON, H R, PRATT-THOMAS
openaire   +2 more sources

Update on Clinical Trials of Losartan With and Without β-Blockers to Block Aneurysm Growth in Patients With Marfan Syndrome: A Review.

JAMA cardiology, 2019
Importance Thoracic aortic aneurysms leading to acute aortic dissections are a major cause of morbidity and mortality despite significant advances in surgical treatment, which remains the main intervention to prevent type A dissections.
Marion A. Hofmann Bowman   +2 more
semanticscholar   +1 more source

The incidence of Marfan syndrome and cardiac anomalies in patients presenting with pectus deformities.

Journal of Pediatric Surgery, 2019
PURPOSE The incidence of Marfan syndrome in the general population is 0.3%. Two-thirds of patients with Marfan syndrome have concurrent pectus deformity.
Christopher A. Behr   +6 more
semanticscholar   +1 more source

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