Literature DB >> 25944702

An increased prevalence of thyroid disease in children with 22q11.2 deletion syndrome.

Andrea L Shugar1,2, Jessica M Shapiro3, Cheryl Cytrynbaum1,2, Stephanie Hedges1, Rosanna Weksberg1,4, Leona Fishman1.   

Abstract

We reviewed the health records of pediatric patients with 22q11.2 deletion syndrome (22q11.2 DS) seen over a 5-year period in our 22q11.2 DS multidisciplinary clinic. We determined the prevalence of thyroid dysfunction in this population, in comparison to general population data. Statistical tests were applied to investigate trends in gender differences, thyroid disease subtype and co-morbid conditions in the patients identified with thyroid disease. Of 169 subjects (92 male, 77 female) 9.5% had overt thyroid disease; of these, 1.8% had hyperthyroidism and 7.7% had hypothyroidism; 42% of patients with subclinical or prodromal thyroid disease progressed to overt disease. Our data indicate that thyroid disease prevalence in the 22q11DS pediatric population is significantly higher than that in the general pediatric population Furthermore, over 1/3 of patients in our study population who presented with subclinical thyroid disease progressed to overt disease, requiring medical therapy. Thyroid disease screening should be incorporated into routine medical management of children with 22q11.2 DS. Guidelines for screening individuals with 22q11.2 DS are presented.
© 2015 Wiley Periodicals, Inc.

Entities:  

Keywords:  22q11 deletion syndrome; Di George syndrome; hypothyroidism; microdeletion; pediatric; prevalence; thyroid disease; velocardiofacial syndrome

Mesh:

Year:  2015        PMID: 25944702     DOI: 10.1002/ajmg.a.37064

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  7 in total

Review 1.  Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiers.

Authors:  Marta Unolt; Paolo Versacci; Silvia Anaclerio; Caterina Lambiase; Giulio Calcagni; Matteo Trezzi; Adriano Carotti; Terrence Blaine Crowley; Elaine H Zackai; Elizabeth Goldmuntz; James William Gaynor; Maria Cristina Digilio; Donna M McDonald-McGinn; Bruno Marino
Journal:  Am J Med Genet A       Date:  2018-04-16       Impact factor: 2.802

Review 2.  Neurodevelopmental outcome in 22q11.2 deletion syndrome and management.

Authors:  Ann Swillen; Edward Moss; Sasja Duijff
Journal:  Am J Med Genet A       Date:  2018-04-25       Impact factor: 2.802

Review 3.  Congenital Hypothyroidism: A 2020-2021 Consensus Guidelines Update-An ENDO-European Reference Network Initiative Endorsed by the European Society for Pediatric Endocrinology and the European Society for Endocrinology.

Authors:  Paul van Trotsenburg; Athanasia Stoupa; Juliane Léger; Tilman Rohrer; Catherine Peters; Laura Fugazzola; Alessandra Cassio; Claudine Heinrichs; Veronique Beauloye; Joachim Pohlenz; Patrice Rodien; Regis Coutant; Gabor Szinnai; Philip Murray; Beate Bartés; Dominique Luton; Mariacarolina Salerno; Luisa de Sanctis; Mariacristina Vigone; Heiko Krude; Luca Persani; Michel Polak
Journal:  Thyroid       Date:  2021-03       Impact factor: 6.568

Review 4.  Hashimoto's Thyroiditis and Graves' Disease in Genetic Syndromes in Pediatric Age.

Authors:  Celeste Casto; Giorgia Pepe; Alessandra Li Pomi; Domenico Corica; Tommaso Aversa; Malgorzata Wasniewska
Journal:  Genes (Basel)       Date:  2021-02-04       Impact factor: 4.096

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

Authors:  Silvia Ricci; Walter Maria Sarli; Lorenzo Lodi; Clementina Canessa; Francesca Lippi; Chiara Azzari; Stefano Stagi
Journal:  Genes (Basel)       Date:  2022-08-28       Impact factor: 4.141

6.  Normal IgH Repertoire Diversity in an Infant with ADA Deficiency After Gene Therapy.

Authors:  Carolyn H Baloh; Samiksha A Borkar; Kai-Fen Chang; Jiqiang Yao; Michael S Hershfield; Suhag H Parikh; Donald B Kohn; Maureen M Goodenow; John W Sleasman; Li Yin
Journal:  J Clin Immunol       Date:  2021-06-28       Impact factor: 8.317

Review 7.  Autoimmune Thyroid Disease in Specific Genetic Syndromes in Childhood and Adolescence.

Authors:  Eleni Magdalini Kyritsi; Christina Kanaka-Gantenbein
Journal:  Front Endocrinol (Lausanne)       Date:  2020-08-19       Impact factor: 5.555

  7 in total

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