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- W2262508291 abstract "Since the identification of the fibrillin‑1 gene as the causal gene for Marfan syndrome, our knowledge of molecular genetics and the applicability of genetic testing for heritable thoracic aneurysms and dissections (H-TAD) in clinical practice have increased substantially. Several new syndromes related to H-TAD have been described and the list of mutated genes in syndromal and nonsyndromal H-TAD is rapidly expanding. This knowledge has led to a significant improvement of our insight into the underlying pathophysiology of H-TAD resulting in new opportunities for targeted treatment, as well as in improved risk stratification. Clinicians involved in the care for H-TAD patients require a basic knowledge of the disease entities and need to be correctly informed on the applicability of genetic testing in their patients and families. Gene‑tailored treatment and management should now be considered as part of good clinical practice. We provide a systematic overview of genetic H-TAD entities and practical recommendations for genetic testing and patient management." @default.
- W2262508291 created "2016-06-24" @default.
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- W2262508291 date "2013-12-16" @default.
- W2262508291 modified "2023-09-23" @default.
- W2262508291 title "New insights into the molecular diagnosis and management of heritable thoracic aortic aneurysms and dissections" @default.
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- W2262508291 doi "https://doi.org/10.20452/pamw.2015" @default.
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