Ventricularpre-excitationand Ebstein anomaly in a patient with Phelan Mc Dermid syndrome: A case report

Ventricularpre-excitationand Ebstein anomaly in a patient with Phelan Mc Dermid syndrome: A case report

Phelan-McDermid syndrome (PMS) or deletion 22q13 syndrome is a rare genetic syndrome resulting from loss of 22q13 region involving the SHANK3 gene. Main features are neonatal hypotonia, global developmental delay, absent to severely delayed speech and minor dysmorphic features. The true incidence re...

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Bibliographic Details
Main Authors: Flavia Caime, Aurora Framcesca Meo, Francesco De Luca, Letteria Bruno, Maria Pia Calabrò, Eloisa Gitto
Format: Article
Language:English
Published: Accademia Peloritana dei Pericolanti 2022-06-01
Series:Atti della Accademia Peloritana dei Pericolanti - Classe di Scienze Medico-Biologiche
Subjects:
ventricular pre-excitation, ebstein’s anomaly, congenital heart disease, genetic syndrome, phelan-mcdermid syndrome
Online Access:https://cab.unime.it/journals/index.php/APMB/article/view/3455

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https://cab.unime.it/journals/index.php/APMB/article/view/3455

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