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

Ricci, Silvia; Sarli, Walter Maria; Lodi, Lorenzo; Canessa, Clementina; Lippi, Francesca; Azzari, Chiara; Stagi, Stefano

Ricci, Silvia; Sarli, Walter Maria; Lodi, Lorenzo; Canessa, Clementina; Lippi, Francesca; Azzari, Chiara; Stagi, Stefano.

Afiliación

Ricci S; Department of Health Sciences, University of Florence, Paediatric Immunology Division, Anna Meyer Children's University Hospital, 50139 Florence, Italy.
Sarli WM; Department of Health Sciences, University of Florence, Paediatric Immunology Division, Anna Meyer Children's University Hospital, 50139 Florence, Italy.
Lodi L; Department of Health Sciences, University of Florence, Paediatric Immunology Division, Anna Meyer Children's University Hospital, 50139 Florence, Italy.
Canessa C; Paediatric Immunology Division, Anna Meyer Children's University Hospital, 50139 Florence, Italy.
Lippi F; Paediatric Immunology Division, Anna Meyer Children's University Hospital, 50139 Florence, Italy.
Azzari C; Department of Health Sciences, University of Florence, Paediatric Immunology Division, Anna Meyer Children's University Hospital, 50139 Florence, Italy.
Stagi S; Department of Health Sciences, University of Florence, Auxoendocrinology Division, Anna Meyer Children's University Hospital, 50139 Florence, Italy.

Genes (Basel) ; 13(9)2022 08 28.

Article en En | MEDLINE | ID: mdl-36140720

Asunto(s)

Síndrome de DiGeorge; Cardiopatías Congénitas; Adolescente; Niño; Estudios de Cohortes; Síndrome de DiGeorge/diagnóstico por imagen; Síndrome de DiGeorge/epidemiología; Síndrome de DiGeorge/genética; Cardiopatías Congénitas/genética; Humanos; Estudios Longitudinales; Tiroxina

Palabras clave

22q11.2 deletion syndrome; Di George syndrome; autoimmune thyroid disease; hyperthyroidism; hypothyroidism; microdeletion; pediatric; thyroid disease; thyroid hypoplasia; thyroid sonography

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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Síndrome de DiGeorge / Cardiopatías Congénitas Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Límite: Adolescent / Child / Humans Idioma: En Revista: Genes (Basel) Año: 2022 Tipo del documento: Article País de afiliación: Italia

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