Left ventricular non-compaction cardiomyopathy: restrictive subtype with MYH7 gene mutation

Oztarhan K., Senturk B., Ucar O.

CARDIOLOGY IN THE YOUNG, cilt.33, ss.810-812, 2023 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 33
  • Basım Tarihi: 2023
  • Doi Numarası: 10.1017/s1047951122002773
  • Dergi Adı: CARDIOLOGY IN THE YOUNG
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, EMBASE, MEDLINE
  • Sayfa Sayıları: ss.810-812
  • İstanbul Üniversitesi Adresli: Evet

Özet

Left ventricular non-compaction is a very rare, still unclassified congenital cardiomyopathy. Nine distinct subtypes of functional and anatomical left ventricular non-compaction have been identified. Studies on the prognosis and mortality of subtypes are ongoing. Our study presented the first restrictive subtype left ventricular non-compaction case with family history and MYH7 gene mutation.