Cardiac involvement of Gorlin-Goltz syndrome: new light among the shadows of an old congenital disorder

Cardiac involvement of Gorlin-Goltz syndrome: new light among the shadows of an old congenital disorder

Mutations in the PTCH1, PTCH2, or SUFU genes cause the hereditary, autosomal dominant Gorlin-Goltz syndrome (GGS), which is characterized by high penetrance and variable expressivity. Although its clinical manifestations are primarily marked by multiple basal cell carcinomas, other endocrine, neuro...

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Bibliographic Details
Main Authors: Mihail Celeski, Andrea Segreti, Annunziata Nusca, Giuseppe Di Gioia, Raffaele Rinaldi, Gian Paolo Ussia, Francesco Grigioni
Format: Article
Language:English
Published: PAGEPress Publications 2025-02-01
Series:Monaldi Archives for Chest Disease
Subjects:
Gorlin-Goltz syndrome
basal cell naevus syndrome
myocarditis
myocardial injury
cardiovascular screening
Online Access:https://www.monaldi-archives.org/macd/article/view/3251
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https://www.monaldi-archives.org/macd/article/view/3251

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