Characterization of Autoimmune Thyroid Disease in a Cohort of 73 Paediatric Patients Affected by 22q11.2 Deletion Syndrome: Longitudinal Single-Centre Study

Background. Chromosome 22q11.2 Deletion Syndrome (22q11.2DS) is the most frequent microdeletion syndrome and is mainly characterized by congenital cardiac defects, dysmorphic features, hypocalcemia, palatal dysfunction, developmental delay, and impaired immune function due to thymic hypoplasia or ap...

Descripción completa

Detalles Bibliográficos
Autores principales: Ricci, Silvia, Sarli, Walter Maria, Lodi, Lorenzo, Canessa, Clementina, Lippi, Francesca, Azzari, Chiara, Stagi, Stefano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9498530/
https://www.ncbi.nlm.nih.gov/pubmed/36140720
http://dx.doi.org/10.3390/genes13091552

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9498530/
https://www.ncbi.nlm.nih.gov/pubmed/36140720
http://dx.doi.org/10.3390/genes13091552

Ejemplares similares