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Growth in Autoimmune Thyroiditis: Clinical Features, Controversies, and Outcomes in the Pediatric Population

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Abstract

Chronic lymphocytic thyroiditis (CLT) is an autoimmune process that is the most common cause of acquired hypothyroidism and can lead to severe growth failure. CLT is a frequent hormone abnormality in pediatrics, being present in up to 2.5% of children. Growth failure from severely low levels of thyroid hormone usually occurs as a late finding, because the onset of symptoms is often insidious. Hypothyroidism from CLT is associated with delayed bone age, and early diagnosis and treatment should preserve final height. Nevertheless, initial treatment with a full replacement dose of levothyroxine has been associated with rapid advancement of the bone age and a compromise in final adult height. Additionally, treatment of CLT with severe bone age delay during puberty may result in a decreased final height. Because of the relatively high incidence of the condition and the non-specific nature of many of the symptoms, physicians caring for children are encouraged to keep a low threshold for checking thyroid function in children. Though data are few, early discovery and treatment of the disease is felt to avoid significant growth effects.

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Abbreviations

AMP:

Adenosine monophosphate

BA:

Bone age

BMI:

Body mass index

CLT:

Chronic lymphocytic thyroiditis

FSH:

Follicle-stimulating hormone

hCG:

Human chorionic gonadotropin

HA:

Height age

HLA:

Human leukocyte antigen

SCH:

Subclinical hypothyroidism

SDS:

Standard deviation score

TRH:

Thyrotropin-releasing hormone

TSBAb:

TSH receptor blocking antibody

TSH:

Thyroid-stimulating hormone

TSI:

Thyroid-stimulating immunoglobulin

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Correspondence to Mark D. DeBoer .

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Demartini, S., DeBoer, M.D. (2012). Growth in Autoimmune Thyroiditis: Clinical Features, Controversies, and Outcomes in the Pediatric Population. In: Preedy, V. (eds) Handbook of Growth and Growth Monitoring in Health and Disease. Springer, New York, NY. https://doi.org/10.1007/978-1-4419-1795-9_158

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  • DOI: https://doi.org/10.1007/978-1-4419-1795-9_158

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