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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
Clinical and echocardiographic study of hypertrophic cardiomyopathy in Tanzania
E E Maro1, M Janabi, R Kaushik
1Muhimbili University College of Health Sciences, PO Box 65202, Dar es Salaam, Tanzania.
Insights
Hypertrophic cardiomyopathy (HCM) is rare in published African reports. Echocardiography revealed HCM in 0.19% of patients, highlighting the need for this diagnostic tool.
Area of Science:
- Cardiology
- Medical Imaging
Background:
- Published reports on hypertrophic cardiomyopathy (HCM) in African populations are scarce.
- Limited access to echocardiography equipment in many African hospitals contributes to underdiagnosis.
Purpose of the Study:
- To determine the prevalence of hypertrophic cardiomyopathy (HCM) in patients referred for echocardiography in Tanzania.
- To emphasize the diagnostic utility of echocardiography for HCM.
Main Methods:
- Retrospective analysis of 6680 echocardiography referrals at Muhimbili National Hospital from June 1998 to October 2002.
- Diagnosis of HCM based on echocardiographic findings.
Main Results:
- Hypertrophic cardiomyopathy (HCM) was diagnosed in 134 (0.19%) patients.
- The mean age of affected patients was 54.8 years, with 67.9% being male.
- Only 5.9% of HCM patients received a correct pre-echocardiography diagnosis due to diverse clinical presentations.
Conclusions:
- Echocardiography is crucial for the accurate diagnosis of hypertrophic cardiomyopathy (HCM).
- Increased availability of echocardiography is essential for early and precise HCM diagnosis in African settings.
- Further research is needed to understand HCM prevalence and characteristics in African populations.
Abstract:
There are few published reports of hypertrophic cardiomyopathy (HCM) in Africans, partly due to lack of Echocardiography machines at most hospitals. Among 6680 patients referred for echocardiography at Muhimbili National Hospital between June 1998 and October 2002, 134 (0.19%) patients had HCM. Their mean age was 54.8+/-14.2 years. In total 67.9% were men and 32.1% were women. Due to the diverse clinical features only eight (5.9%) patients had a correct diagnosis of HCM prior to their ECHO. The important role of echocardiography in the diagnosis of HCM is stressed with a plea for the increasing availability of this non-invasive technique for early and accurate diagnosis.
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