Aneurysms-Osteoarthritis Syndrome: SMAD3 Gene Mutations
by Denise van der Linde, Jolien Roos-Hesselink, Bart L. Loeys
Aneurysms-Osteoarthritis Syndrome: SMAD3 Gene Mutations is a first-of-its-kind compilation of the genetic discovery, research, and care associated with AOS. With the field of genetically triggered aortopathies growing, this important reference will compile the newest discoveries in this field, allowing cardiologists, cardio-thoracic surgeons, clinical geneticists, vascular surgeons, orthopedic surgeons, and researchers to gain the knowledge they need without having to gather the data from various sources.
Coverage includes genotype and phenotype correlations, the functional role of SMAD3, and insights into the role of TGFbeta signaling in aortic disease. The book will increase knowledge about AOS, providing awareness and better patient care for this aggressive disease.
- Covers Aneurysms-Osteoarthritis Syndrome, from genetic discovery to patient care
- Contains clinical management guidance on optimal cardiovascular treatments and surgery
- Explains the autosomal dominant syndromes caused by mutations in the SMAD3 gene
- Identifies the key features of this syndrome, including arterial aneurysms and tortuosity, early onset arthritis, and mild craniofacial features
Discuss Aneurysms-Osteoarthritis Syndrome: SMAD3 Gene Mutations with other readers
Join or start a book club for Aneurysms-Osteoarthritis Syndrome: SMAD3 Gene Mutations on Readfeed. Live chat, shared reading progress, and AI discussion questions — free to get started.
Frequently asked questions
How do I join a book club for Aneurysms-Osteoarthritis Syndrome: SMAD3 Gene Mutations?
Sign up free on Readfeed, then browse public clubs or start your own club with Aneurysms-Osteoarthritis Syndrome: SMAD3 Gene Mutations as the current read. Invite friends with a share link and discuss together with live chat and AI discussion questions.
Can I discuss Aneurysms-Osteoarthritis Syndrome: SMAD3 Gene Mutations with other readers online?
Yes. Readfeed book clubs let you chat live, share progress, and join discussions about Aneurysms-Osteoarthritis Syndrome: SMAD3 Gene Mutations with readers worldwide — whether your club is virtual, in-person, or hybrid.
Is Readfeed free?
Yes. Creating an account and joining book clubs is free. Sign up to find readers who love the same books and start discussing today.