Marfan Syndrome Latest Advances

A Case of FBN1-Related Early Onset Marfan Syndrome with Multi-Suture Craniosynostosis.

Journal: The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association

Published: June 18, 2026

Body size in young adulthood is associated with thoracic aortic events later in life.

Journal: Scandinavian cardiovascular journal : SCJ

Published: June 16, 2026

Lymphatic dysfunction and ZFP36 deficiency contribute to myxomatous valve degeneration in Marfan Syndrome mice.

Journal: The Journal of clinical investigation

Published: June 11, 2026

Nuclear SUN2 coordinates endothelial cell-matrix interactions to regulate blood vessel homeostasis and barrier function.

Journal: bioRxiv : the preprint server for biology

Published: June 04, 2026

Growth Arrest of Thoracic Aortic Aneurysms in Aging Marfan Mice.

Journal: American journal of physiology. Heart and circulatory physiology

Published: June 01, 2026

Beyond the aorta: Marfan syndrome as a diffuse arteriopathy.

Journal: Heart (British Cardiac Society)

Published: May 26, 2026

Correlations of aortic dimensions, pulmonary artery, and body surface area in pediatric Marfan

Journal: Archivos de cardiologia de Mexico

Published: May 18, 2026

Successful Staged Total Aortic Replacement in a Young Patient with Marfan Syndrome:Report of a Case

Journal: Kyobu geka. The Japanese journal of thoracic surgery

Published: May 07, 2026

Spontaneously resolved pseudoaneurysm after valve-sparing aortic root replacement in Marfan syndrome: a case report - CORRIGENDUM.

Journal: Cardiology in the young

Published: May 05, 2026

Generation of induced pluripotent stem cell lines from three Marfan syndrome patients carrying mutations in the fibrillin-1 gene.

Journal: Stem cell research

Published: May 05, 2026

Non-necrotising Scleritis and Spherophakia in Marfan Syndrome: A Rare Situation Adhering to Hickam's Dictum.

Journal: Kathmandu University medical journal (KUMJ)

Published: April 23, 2026

Outcomes of Type B Dissection in Marfan Syndrome: The Cornell Aortic Aneurysm Registry.

Journal: Journal of the American Heart Association

Published: April 22, 2026

Marfan Syndrome Latest Advances

Find the Latest Research About Marfan Syndrome

A Case of FBN1-Related Early Onset Marfan Syndrome with Multi-Suture Craniosynostosis.

A Case of FBN1-Related Early Onset Marfan Syndrome with Multi-Suture Craniosynostosis.

Body size in young adulthood is associated with thoracic aortic events later in life.

Body size in young adulthood is associated with thoracic aortic events later in life.

Lymphatic dysfunction and ZFP36 deficiency contribute to myxomatous valve degeneration in Marfan Syndrome mice.

Lymphatic dysfunction and ZFP36 deficiency contribute to myxomatous valve degeneration in Marfan Syndrome mice.

Nuclear SUN2 coordinates endothelial cell-matrix interactions to regulate blood vessel homeostasis and barrier function.

Nuclear SUN2 coordinates endothelial cell-matrix interactions to regulate blood vessel homeostasis and barrier function.

Growth Arrest of Thoracic Aortic Aneurysms in Aging Marfan Mice.

Growth Arrest of Thoracic Aortic Aneurysms in Aging Marfan Mice.

Beyond the aorta: Marfan syndrome as a diffuse arteriopathy.

Beyond the aorta: Marfan syndrome as a diffuse arteriopathy.

Correlations of aortic dimensions, pulmonary artery, and body surface area in pediatric Marfan

Correlations of aortic dimensions, pulmonary artery, and body surface area in pediatric Marfan

Successful Staged Total Aortic Replacement in a Young Patient with Marfan Syndrome:Report of a Case

Successful Staged Total Aortic Replacement in a Young Patient with Marfan Syndrome:Report of a Case

Spontaneously resolved pseudoaneurysm after valve-sparing aortic root replacement in Marfan syndrome: a case report - CORRIGENDUM.

Spontaneously resolved pseudoaneurysm after valve-sparing aortic root replacement in Marfan syndrome: a case report - CORRIGENDUM.

Generation of induced pluripotent stem cell lines from three Marfan syndrome patients carrying mutations in the fibrillin-1 gene.

Generation of induced pluripotent stem cell lines from three Marfan syndrome patients carrying mutations in the fibrillin-1 gene.

Non-necrotising Scleritis and Spherophakia in Marfan Syndrome: A Rare Situation Adhering to Hickam's Dictum.

Non-necrotising Scleritis and Spherophakia in Marfan Syndrome: A Rare Situation Adhering to Hickam's Dictum.

Outcomes of Type B Dissection in Marfan Syndrome: The Cornell Aortic Aneurysm Registry.

Outcomes of Type B Dissection in Marfan Syndrome: The Cornell Aortic Aneurysm Registry.