Beckwith–Wiedemann syndrome: Clinical, histopathological and molecular study of two Tunisian patients and review of literature

Beckwith–Wiedemann syndrome: Clinical, histopathological and molecular study of two Tunisian patients and review of literature

Abstract Background Beckwith–Wiedemann syndrome (BWS) is a rare overgrowth syndrome characterized by congenital malformations and predisposition to embryonic tumors. Loss of methylation of imprinting center 2 (IC2) is the most frequent alteration and rarely associated with tumors compared to paterna...

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Autores principales: Hela Sassi, Yasmina Elaribi, Houweyda Jilani, Imen Rejeb, Syrine Hizem, Molka Sebai, Nadia Kasdallah, Habib Bouthour, Samia Hannachi, Jasmin Beygo, Ali Saad, Karin Buiting, Dorra H’mida Ben‐Brahim, Lamia BenJemaa
Formato: article
Lenguaje:EN
Publicado: Wiley 2021
Materias:
adrenocortical tumors
Beckwith–Wiedemann syndrome
correlation
epigenetic
genomic imprinting
Genetics
QH426-470
Acceso en línea:https://doaj.org/article/fc40ee2cb6c545c19d90a77e319e55ec
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https://doaj.org/article/fc40ee2cb6c545c19d90a77e319e55ec

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