| Abstrakt: |
Researchers from the Department of Cardiology in Lagos, Nigeria have published a study on monogenic hypertension syndromes, which are caused by a single genetic mutation and present with severe hypertension, distinct laboratory abnormalities, and a positive family history. These syndromes are often misdiagnosed as essential hypertension, so the paper aims to educate doctors on recognizing and managing these conditions early to prevent organ damage. The researchers emphasize the importance of genetic testing facilities in aiding the earlier diagnosis of these conditions. The full article can be accessed for free through the provided link. [Extracted from the article] |
