Risk of thyroid neoplasms in patients with 22q11.2 deletion and DiGeorge-like syndromes: an insight for follow-up

Risk of thyroid neoplasms in patients with 22q11.2 deletion and DiGeorge-like syndromes: an insight for follow-up

IntroductionThe chromosome 22q11.2 deletion syndrome comprises phenotypically similar diseases characterized by abnormal development of the third and fourth branchial arches, resulting in variable combinations of congenital heart defects, dysmorphisms, hypocalcemia, palatal dysfunction, developmenta...

Ausführliche Beschreibung

Bibliographische Detailangaben
Hauptverfasser: Walter Maria Sarli, Silvia Ricci, Lorenzo Lodi, Federica Cavone, Lucia Pacillo, Carmela Giancotta, Graziamaria Ubertini, Giampiero Baroncelli, Caterina Cancrini, Chiara Azzari, Stefano Stagi
Format: Artikel
Sprache:English
Veröffentlicht: Frontiers Media S.A. 2023-08-01
Schriftenreihe:Frontiers in Endocrinology
Schlagworte:
thyroid cancer
thyroid nodules
22q11 deletion syndrome
DiGeorge
genetic syndrome
Online Zugang:https://www.frontiersin.org/articles/10.3389/fendo.2023.1209577/full

Online

https://www.frontiersin.org/articles/10.3389/fendo.2023.1209577/full

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