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

INTRODUCTION: The 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, developmen...

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Detalles Bibliográficos
Autores principales: Sarli, Walter Maria, Ricci, Silvia, Lodi, Lorenzo, Cavone, Federica, Pacillo, Lucia, Giancotta, Carmela, Ubertini, Graziamaria, Baroncelli, Giampiero, Cancrini, Caterina, Azzari, Chiara, Stagi, Stefano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10450035/
https://www.ncbi.nlm.nih.gov/pubmed/37635986
http://dx.doi.org/10.3389/fendo.2023.1209577

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10450035/
https://www.ncbi.nlm.nih.gov/pubmed/37635986
http://dx.doi.org/10.3389/fendo.2023.1209577

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