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

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...

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Bibliographic Details
Main Authors: Silvia Ricci, Walter Maria Sarli, Lorenzo Lodi, Clementina Canessa, Francesca Lippi, Chiara Azzari, Stefano Stagi
Format: Article
Language:English
Published: MDPI AG 2022-08-01
Series:Genes
Subjects:
22q11.2 deletion syndrome
Di George syndrome
hypothyroidism
hyperthyroidism
microdeletion
pediatric
Online Access:https://www.mdpi.com/2073-4425/13/9/1552

Internet

https://www.mdpi.com/2073-4425/13/9/1552

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