An increased prevalence of thyroid disease in children with 22q11.2 deletion syndrome-Reference-Cited by-同舟云学术

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

Published:2015-05-05 Issue:7 Volume:167 Page:1560-1564
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Shugar Andrea L.¹²,Shapiro Jessica M.³,Cytrynbaum Cheryl¹²,Hedges Stephanie¹,Weksberg Rosanna¹⁴,Fishman Leona¹

Affiliation:

1. Division of Clinical & Metabolic Genetics; The Hospital for Sick Children; Toronto ON Canada

2. Department of Molecular Genetics; University of Toronto; Toronto ON Canada

3. School of Medicine; University of Queensland; Brisbane Queensland Australia

4. Institute of Medical Science; University of Toronto; Toronto ON Canada

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.37064/fullpdf

Reference19 articles.

1. Practical guidelines for managing patients with 22q11.2 deletion syndrome;Bassett;J Pediatr,2011

2. Neuropsychiatric aspects of pediatric thyrotoxicosis;Bhatara;Indian J Pediatr,1999

3. Prevalence of thyroid disease, thyroid dysfunction and thyroid peroxidase antibodies in a large, unselected population;Bjoro;Eur J Endocrinol,2000

4. Autoimmune thyroid diseases in children;Cappa;J Thyroid Res,2011

5. Thyroid gland and carotid artery anomalies in 22q11.2 deletion syndromes;de Almeida;Laryngoscope,2009

Cited by 25 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Understanding the Variability of 22q11.2 Deletion Syndrome: The Role of Epigenetic Factors;Genes;2024-02-29

2. Impact of high‐risk prenatal screening results for 22q11.2 deletion syndrome on obstetric and neonatal management: Secondary analysis from the SMART study;Prenatal Diagnosis;2023-12

3. Risk of thyroid neoplasms in patients with 22q11.2 deletion and DiGeorge-like syndromes: an insight for follow-up;Frontiers in Endocrinology;2023-08-10

4. Chromosome 22q11.2 Deletion Syndrome: A Comprehensive Review of Molecular Genetics in the Context of Multidisciplinary Clinical Approach;International Journal of Molecular Sciences;2023-05-05

5. Updated clinical practice recommendations for managing children with 22q11.2 deletion syndrome;Genetics in Medicine;2023-03

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