Dilated Cardiomyopathy Phenotype-Associated Left Ventricular Noncompaction and Congenital Long QT Syndrome Type-2 in Infants With KCNH2 Gene Mutation: Anesthetic Considerations

Madan Mohan Maddali; Eapen Thomas; Ismail Abdullah Al Abri; Malay Hemantlal Patel; Salim Nasser Al Maskari; Mohammed Ismail Al Yamani

doi:10.1053/j.jvca.2022.05.016

Dilated Cardiomyopathy Phenotype-Associated Left Ventricular Noncompaction and Congenital Long QT Syndrome Type-2 in Infants With KCNH2 Gene Mutation: Anesthetic Considerations

J Cardiothorac Vasc Anesth. 2022 Sep;36(9):3662-3667. doi: 10.1053/j.jvca.2022.05.016. Epub 2022 May 16.

Authors

Madan Mohan Maddali¹, Eapen Thomas², Ismail Abdullah Al Abri², Malay Hemantlal Patel³, Salim Nasser Al Maskari², Mohammed Ismail Al Yamani⁴

Affiliations

¹ Department of Cardiac Anesthesia, National Heart Center, Royal Hospital, Muscat, Oman. Electronic address: [email protected].
² Department of Cardiology, National Heart Center, Royal Hospital, Muscat, Oman.
³ Department of Cardiac Anesthesia, National Heart Center, Royal Hospital, Muscat, Oman.
⁴ Department of Cardiothoracic Surgery, National Heart Center, Royal Hospital, Muscat, Oman.

PMID: 35718623
DOI: 10.1053/j.jvca.2022.05.016

No abstract available

Keywords: cardiomyopathies; channelopathies/genetics; isolated noncompaction of the ventricular myocardium; long QT syndrome/genetics; long QT syndrome/therapy; phenotype.

Publication types

Case Reports

MeSH terms

Anesthetics*
Cardiomyopathies*
Cardiomyopathy, Dilated* / complications
Cardiomyopathy, Dilated* / diagnostic imaging
Cardiomyopathy, Dilated* / genetics
ERG1 Potassium Channel / genetics
Heart Defects, Congenital*
Humans
Long QT Syndrome* / complications
Long QT Syndrome* / diagnosis
Long QT Syndrome* / genetics
Mutation
Phenotype

Substances

Anesthetics
ERG1 Potassium Channel
KCNH2 protein, human