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Aneurysms Osteoarthritis Syndrome SMAD 3 Gene Mutations

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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

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Ketersediaan

Informasi Detail

Judul Seri

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No. Panggil

616.72 DEN a

Penerbit

Amsterdam : Academic Press Is an Imprint of Elsevier., 2017

Deskripsi Fisik

xiii, 163 hlm ; ilus. ; 23 cm

Bahasa

English

ISBN/ISSN

9780128027080

Klasifikasi

616.72

Tipe Isi

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Tipe Media

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Tipe Pembawa

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Edisi

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Subjek

Aneurysms-Osteoarthritis

Info Detail Spesifik

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Pernyataan Tanggungjawab

Denise Van Der Linde

Versi lain/terkait

Lampiran Berkas

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