Work

Marfan syndrome and multiple myeloma: A coincidence or tendency?

Year: 2024

Type: article

Abstract: Marfan Syndrome (MFS) is an autosomal dominant connective tissue disorder characterized by musculoskeletal, ocular, and cardiovascular abnormalities. It results from a mutation in the fibrillin-1 gene, leading to its deficiency and often causing overactivation of the TGF-β signaling pathway, which may contribute to cancer development.

Source: Journal of Clinical Images and Medical Case Reports

DOI: 10.52768/2766-7820/3293

Author: Atakan Turgutkaya

Institution: Adnan Menderes University

Language: English

Topic: Connective tissue disorders research

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: bronze

OpenAlex ID: W4407177990