Neonatal death of siblings with Uhl’s disease and KCNH2 mutation - A rare association

Uhl’s disease is a rare disorder secondary to the uncontrolled destruction of right ventricular myocytes during the perinatal period. We present here the case of a 1-month-old child who died suddenly of Uhl’s disease, which was only diagnosed at autopsy and histological examination. From an anamnest...

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Bibliographic Details

Published in:	Annals of Pediatric Cardiology
Main Authors:	Francesco Ventura, Rosario Barranco, Francesca Buffelli, Ezio Fulcheri, Domenico Coviello, Antonella Palmieri
Format:	Article
Language:	English
Published:	Wolters Kluwer Medknow Publications 2024-11-01
Subjects:	autopsy genetic analysis kcnh2 gene myocardial disease uhl’s disease
Online Access:	https://journals.lww.com/10.4103/apc.apc_122_24