CAV3 Variants among Iranian Patients with Cardiomyopathy

Publish Year: 1398
نوع سند: مقاله کنفرانسی
زبان: English
View: 457

نسخه کامل این Paper ارائه نشده است و در دسترس نمی باشد

  • Certificate
  • من نویسنده این مقاله هستم

این Paper در بخشهای موضوعی زیر دسته بندی شده است:

استخراج به نرم افزارهای پژوهشی:

لینک ثابت به این Paper:

شناسه ملی سند علمی:

BSIPD01_032

تاریخ نمایه سازی: 5 بهمن 1398

Abstract:

Introduction:Cardiomyopathy is one of the major defects of heart failure which causes heart disability to pump blood for metabolic activities. Some types of Cardiomyopathy are Hypertrophic (HCM), Restrictive (RCM) and Dilated (DCM), which DCM is the most common inherited type. Here we studied CAV3 gene variants as a sarcomeric gene; make an important role in demonstration of this disease.Materials & Methods: All entrants were selected from cardiomyopathy patients who have identified by Echocardiography results. Blood samples were collected and after conducting PCR, CAV3 was sequenced.Results: This study showed that variants of CAV3 gene play no significant role in demonstration of cardiomyopathy.Conclusion & discussion: The result didn’t show any specific variant on CAV3, but further studies on involved genes in cardiomyopathy are beneficial and necessary way of diagnosis and treatment

Authors

Bahareh Ghanadi

Department of Genetics, Faculty of Advanced Science and Technology, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran

Nejat Mahdieh

Cardiogenetic Research Laboratory, Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, Iran.

Seyed Hamid Jamaldini

Medical Genomics Research Center, Tehran Medical Sciences Branch, Islamic Azad University, Tehran, Iran.

Sepideh Taghavi

Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, Iran.

Bahareh Rabbani

Cardiogenetics Research Laboratory, Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, Iran