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A Case Report on the Atypical Presentation of Hypertrophic Cardiomyopathy (HOCM) in a 19-Year-Old Female.
Alhazmi, Ahmed; Almatrafi, Shahad B; Abdulwahab, Rahaf A; Alzahrani, Asma; Sindi, Ghufran.
Afiliação
  • Alhazmi A; Cardiology, King Abdullah Medical City, Makkah, SAU.
  • Almatrafi SB; College of Medicine, Umm Al-Qura University, Al-Abdia Main Campus, Makkah, SAU.
  • Abdulwahab RA; Medicine and Surgery, Umm Al-Qura University, Makkah, SAU.
  • Alzahrani A; College of Medicine, Umm Al-Qura University, Al-Abdia Main Campus, Makkah, SAU.
  • Sindi G; College of Medicine, Umm Al-Qura University, Al-Abdia Main Campus, Makkah, SAU.
Cureus ; 14(12): e33136, 2022 Dec.
Article em En | MEDLINE | ID: mdl-36601155
ABSTRACT
Atypical hypertrophic cardiomyopathy (HOCM) is a relatively rare genetic disorder that can affect the left ventricular system. HOCM can lead to various cardiac issues such as sudden cardiac death (SCD). We report a case of a 19-year-old female who was referred to a cardiology clinic after presenting with bi-ventricular hypertrophy on an echocardiogram (ECHO). Results from screening tests for infiltrative diseases and an iron panel came negative. The patient was asymptomatic, with no functional limitations and no family history of any cardiac disease or sudden death. In conclusion, HOCM can present with an atypical pattern, such as biventricular hypertrophy, and has been linked to SCD; therefore, it is important to be aware of this condition and take the necessary precautions to prevent it.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article