E-ISSN 2534-9821
 

Case Report 


Rare case of aortopathy revealing hypertrophic cardiomyopathy

Meriem El Mousaid, Hanae Charif, Noelle Mahoungou-Mackonia, Imad Nouamou, Meryem Haboub, Leila Azzouzi, Rachida Habbal.

Abstract
Hypertrophic cardiomyopathy (HCM) is the most prevalent (0.2%) heritable, genetic cardiovascular disease. Aortopathies also represent a spectrum of familial inheritance with prevalence of ~4%. Previous research evaluating characteristics of the aorta in HCM patients have demonstrated increased vascular stiffness and differences in aortic elastic properties compared to healthy controls. However, a prevalence of aortopathy in HCM patients has not been previously described and a potential relationship between HCM and aortic dilation has not been established limited by relatively small patient cohorts. We report the case of a 64 years old patient who was admitted to our cardiology department for the treatment of obstructive hypertrophic cardiomyopathy associated with anevrysmal dilation of the ascending aorta.

Key words: Hypertrophic cardiomyopathy, aortopathy, genetic disease, aortic dilation


 
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How to Cite this Article
Pubmed Style

Mousaid ME, Charif H, Mahoungou-Mackonia N, Nouamou I, Haboub M, Azzouzi L, Habbal R, . Rare case of aortopathy revealing hypertrophic cardiomyopathy. Int J Med Rev Case Rep. 2022; 6(16): 27-31. doi:10.5455/IJMRCR.172-1657198203


Web Style

Mousaid ME, Charif H, Mahoungou-Mackonia N, Nouamou I, Haboub M, Azzouzi L, Habbal R, . Rare case of aortopathy revealing hypertrophic cardiomyopathy. https://www.mdpub.net/?mno=80258 [Access: January 14, 2023]. doi:10.5455/IJMRCR.172-1657198203


AMA (American Medical Association) Style

Mousaid ME, Charif H, Mahoungou-Mackonia N, Nouamou I, Haboub M, Azzouzi L, Habbal R, . Rare case of aortopathy revealing hypertrophic cardiomyopathy. Int J Med Rev Case Rep. 2022; 6(16): 27-31. doi:10.5455/IJMRCR.172-1657198203



Vancouver/ICMJE Style

Mousaid ME, Charif H, Mahoungou-Mackonia N, Nouamou I, Haboub M, Azzouzi L, Habbal R, . Rare case of aortopathy revealing hypertrophic cardiomyopathy. Int J Med Rev Case Rep. (2022), [cited January 14, 2023]; 6(16): 27-31. doi:10.5455/IJMRCR.172-1657198203



Harvard Style

Mousaid, M. E., Charif, H., Mahoungou-Mackonia, N., Nouamou, I., Haboub, M., Azzouzi, L., Habbal, R. & (2022) Rare case of aortopathy revealing hypertrophic cardiomyopathy. Int J Med Rev Case Rep, 6 (16), 27-31. doi:10.5455/IJMRCR.172-1657198203



Turabian Style

Mousaid, Meriem El, Hanae Charif, Noelle Mahoungou-Mackonia, Imad Nouamou, Meryem Haboub, Leila Azzouzi, Rachida Habbal, and . 2022. Rare case of aortopathy revealing hypertrophic cardiomyopathy. International Journal of Medical Reviews and Case Reports, 6 (16), 27-31. doi:10.5455/IJMRCR.172-1657198203



Chicago Style

Mousaid, Meriem El, Hanae Charif, Noelle Mahoungou-Mackonia, Imad Nouamou, Meryem Haboub, Leila Azzouzi, Rachida Habbal, and . "Rare case of aortopathy revealing hypertrophic cardiomyopathy." International Journal of Medical Reviews and Case Reports 6 (2022), 27-31. doi:10.5455/IJMRCR.172-1657198203



MLA (The Modern Language Association) Style

Mousaid, Meriem El, Hanae Charif, Noelle Mahoungou-Mackonia, Imad Nouamou, Meryem Haboub, Leila Azzouzi, Rachida Habbal, and . "Rare case of aortopathy revealing hypertrophic cardiomyopathy." International Journal of Medical Reviews and Case Reports 6.16 (2022), 27-31. Print. doi:10.5455/IJMRCR.172-1657198203



APA (American Psychological Association) Style

Mousaid, M. E., Charif, H., Mahoungou-Mackonia, N., Nouamou, I., Haboub, M., Azzouzi, L., Habbal, R. & (2022) Rare case of aortopathy revealing hypertrophic cardiomyopathy. International Journal of Medical Reviews and Case Reports, 6 (16), 27-31. doi:10.5455/IJMRCR.172-1657198203