A rare association of central hypothyroidism and adrenal insufficiency in a boy with Williams-Beuren syndrome
Author:
Affiliation:
1. Department of Paediatric Endocrinology, Alder Hey Children's Hospital NHS Trust, Liverpool, UK.
Publisher
Korean Society of Pediatric Endocrinology
Subject
Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology and Child Health
Link
https://synapse.koreamed.org/pdf/10.6065/apem.2017.22.1.65
Reference17 articles.
1. Williams-Beuren syndrome:genes and mechanisms
2. Prevalence Estimation of Williams Syndrome
3. Natural history of Williams syndrome: Physical characteristics
4. Endocrine dysfunctions in children with Williams-Beuren syndrome
5. Growth Hormone Deficiency in a Child with Williams-Beuren Syndrome. The Response to Growth Hormone Therapy
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1. Combined use of thyroid stimulating hormone plus free thyroxine levels and gestational age at birth for the prediction of neonatal hypothyroidism and associated risk factors;Experimental and Therapeutic Medicine;2020-10-15
2. Autoimmune Thyroid Disease in Specific Genetic Syndromes in Childhood and Adolescence;Frontiers in Endocrinology;2020-08-19
3. Williams Syndrome, Human Self-Domestication, and Language Evolution;Frontiers in Psychology;2019-03-18
4. Central adrenal insufficiency in children and adolescents;Best Practice & Research Clinical Endocrinology & Metabolism;2018-08
5. De Novo Synthesis of Elastin by Exogenous Delivery of Synthetic Modified mRNA into Skin and Elastin-Deficient Cells;Molecular Therapy - Nucleic Acids;2018-06
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