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Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...
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Fibromuscular dysplasia: Challenges for the current classification

Marialuisa Zedde1, Maria Simona Stoenoiu2, Alexandre Persu3,4

  • 1Neurology Unit, Stroke Unit, Azienda Unità Sanitaria Locale-IRCCS Di Reggio Emilia, Viale Risorgimento 80, 42123, Reggio Emilia, Italy. zedde.marialuisa@ausl.re.it.

Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
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PubMed
Summary

No abstract available in PubMed .

Keywords:
FMDFibromuscular dysplasiaInternal carotid arteryOutpouchStroke

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