Marfan syndrome (MFS) is a rare congenital disorder of the connective tissue, leading to
thoracic aortic aneurysms (TAA) and dissection, among other complications. Currently, the …

Marfan syndrome (MFS) is an autosomal dominant genetic disorder caused by mutations in
the fibrillin-1 gene. Acute aortic dissection is the leading cause of death in patients suffering …

Marfan syndrome (MFS) is a connective tissue disorder caused by FBN1 gene mutations
leading to TGF-β signaling hyperactivation, vascular wall weakness, and thoracic aortic …

Women undergoing infertility treatment are routinely subjected to one or more tests of
ovarian reserve. Therefore, an adequate assessment of the ovarian reserve is necessary for …

Marfan syndrome (MFS) is a connective tissue disease caused by mutations in the FBN1
gene, leading to alterations in the extracellular matrix microfibril assembly and the early …

Background In patients with left heart failure, micro-RNAs (miRNAs) have been shown to be
of diagnostic and prognostic value. The present study aims to identify those miRNAs in …

Marfan syndrome (MFS) is one of the most common inherited disorders of connective tissue
caused by mutations of the fibrillin-1 gene (FBN1). Vascular abnormalities, such as the …

Background: Turner Syndrome (TS) is a relatively rare X-chromosomal disease with
increased cardiovascular morbidity and mortality. This study aimed to identify whether the …

Background Turner syndrome (TS) is a chromosomal disorder, in which a female is partially
or entirely missing one of the two X chromosomes, with a prevalence of 1: 2500 live female …

Marfan syndrome (MFS) is a hereditary disease with high mortality. This study aimed to
explore peripheral blood potential markers and underlying mechanisms in MFS via a series …