New case of thyroid dysgenesis and clinical signs of hypothyroidism in Williams syndrome

Author:

Bini Rita,Pela Ivana

Publisher

Wiley

Subject

Genetics(clinical)

Reference8 articles.

1. Congenital anomalies associated with hypothyroidism.

2. Thyroid hemiagenesis and elevated thyrotropin levels in a child with Williams syndrome

3. 1994. Aspetti auxologici ed endocrinologici. In: editors. Il bambino con sindrome di Williams. Milano: Franco Angeli. pp 59-64.

4. Williams-Beuren syndrome:genes and mechanisms

5. 2000. Disorders of the thyroid gland. In: editors. Nelson textbook of pediatrics. Philadelphia: WB Saunders Company. pp 1696-1714.

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1. Autoimmune Thyroid Disease in Specific Genetic Syndromes in Childhood and Adolescence;Frontiers in Endocrinology;2020-08-19

2. Thyroid evaluation of children and adolescents with Williams syndrome in Zhejiang Province;Journal of Pediatric Endocrinology and Metabolism;2017-11-27

3. Seven cases with Williams-Beuren syndrome: endocrine evaluation and long-term follow-up;Journal of Pediatric Endocrinology and Metabolism;2017-01-01

4. Developmental Abnormalities of the Thyroid;Genetic Diagnosis of Endocrine Disorders;2016

5. Bilateral vocal cord paralysis and hypothyroidism as presenting symptoms of Williams–Beuren syndrome: A case report;International Journal of Pediatric Otorhinolaryngology;2015-09

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