Abstract
Subclinical hyperthyroidism (SH) is defined as serum thyroid-stimulating hormone (TSH) below the lower limit of the reference range in the presence of normal free T4 and free T3 levels. Depending on the degree of TSH suppression, SH could be defined as mild (TSH, 0.1–0.45 mU/L) or severe (TSH<0.1 mU/L). Patients with SH are often asymptomatic when symptoms are present, they are similar to the symptoms in patients with overt hyperthyroidism, although they are usually milder. The management of the SH is uncertain and should be individualized. We present this review after an extensive literature search and long-standing clinical experience. This review provides the prevalence, causes, clinical presentation, investigation, and therapeutic approach of SH in children.
Funding source: No fund
Funding source: No Fund
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Research funding: None declared.
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Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.
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Competing interests: Authors state no conflict of interest.
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Informed consent: Not applicable.
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Ethical approval: Not applicable.
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© 2022 Walter de Gruyter GmbH, Berlin/Boston
Articles in the same Issue
- Frontmatter
- Reviews
- Approach to nutritional rickets
- Subclinical hyperthyroidism in children
- Original Articles
- Can thyroid elastography with ultrasound be used to stage children with Hashimoto’s thyroiditis?
- Congenital hypothyroidism in children with eutopic gland or thyroid hemiagenesis: prognostic factors for transient vs. permanent hypothyroidism
- Comparison of developmental outcomes in children with permanent and transient congenital hypothyroidism
- Impact of overweight and obesity on epicardial adipose tissue in children with type 1 diabetes
- Peripheral arterial disease among children with type 1 diabetes mellitus in a Nigerian teaching hospital
- The WHO-5 well-being questionnaire in type 1 diabetes: screening for depression in pediatric and young adult subjects
- Clinical correlation of 2D shear wave elastography findings in children with type 1 diabetes mellitus without autoimmune thyroiditis
- Molecular analysis of MKRN3 gene in Turkish girls with sporadic and familial idiopathic central precocious puberty
- Case Reports
- ALG11-CDG: novel variant and review of the literature
- Betamethasone cream to treat diapers rash causing Cushing syndrome
- Rapid-onset obesity, hypothalamic dysfunction, hypoventilation, and autonomic dysregulation syndrome – neuro-endocrine tumours (ROHHAD-NET): case series and learning points
- Lathosterolosis: a rare cholesterol metabolism disorder with a wide range of clinical variability
- Urea as safe treatment for hyponatremia due to syndrome of inappropriate antidiuretic hormone in infant with solitary central incisor and neurofibromatosis-1
Articles in the same Issue
- Frontmatter
- Reviews
- Approach to nutritional rickets
- Subclinical hyperthyroidism in children
- Original Articles
- Can thyroid elastography with ultrasound be used to stage children with Hashimoto’s thyroiditis?
- Congenital hypothyroidism in children with eutopic gland or thyroid hemiagenesis: prognostic factors for transient vs. permanent hypothyroidism
- Comparison of developmental outcomes in children with permanent and transient congenital hypothyroidism
- Impact of overweight and obesity on epicardial adipose tissue in children with type 1 diabetes
- Peripheral arterial disease among children with type 1 diabetes mellitus in a Nigerian teaching hospital
- The WHO-5 well-being questionnaire in type 1 diabetes: screening for depression in pediatric and young adult subjects
- Clinical correlation of 2D shear wave elastography findings in children with type 1 diabetes mellitus without autoimmune thyroiditis
- Molecular analysis of MKRN3 gene in Turkish girls with sporadic and familial idiopathic central precocious puberty
- Case Reports
- ALG11-CDG: novel variant and review of the literature
- Betamethasone cream to treat diapers rash causing Cushing syndrome
- Rapid-onset obesity, hypothalamic dysfunction, hypoventilation, and autonomic dysregulation syndrome – neuro-endocrine tumours (ROHHAD-NET): case series and learning points
- Lathosterolosis: a rare cholesterol metabolism disorder with a wide range of clinical variability
- Urea as safe treatment for hyponatremia due to syndrome of inappropriate antidiuretic hormone in infant with solitary central incisor and neurofibromatosis-1