A Rare Cause of Thyroid Hormone Abnormalities in an Adolescent: A Case Report of SBP2 (SECISBP2) Deficiency
Year: 2026
Type: article
Study design: Case Report
Abstract: Introduction: Selenocysteine insertion sequence (SECIS)-binding protein 2 (SBP2) (SECISBP2) is essential for selenoprotein synthesis. Selenoproteins play critical roles in cellular redox homeostasis, antioxidant defense, and thyroid hormone metabolism. Deiodinases (DIOs) are selenoenzymes that catalyze the deiodination of iodothyronine and are important for thyroid hormone activation and inactivation. Mutations in SBP2, which facilitates the incorporation of selenium into selenoproteins, lead to defective production of DIOs. Case Presentation: A 13-year-and-6-month-old female patient presented with constipation and abnormal thyroid function tests. Laboratory tests revealed elevated free T4 (25.5 ng/L), normal TSH (1.2 mIU/L), low free T3 (2.3 ng/L), and decreased serum selenium level (14.37 μg/L). The patient exhibited speech and language delay, along with learning difficulties. These findings suggested SBP2 deficiency. Genetic analysis revealed a previously reported homozygous pathogenic variant, c.358C>T (p.Arg120Ter) in the SECISBP2 gene. Conclusion: This case highlights the importance of considering SBP2 deficiency in patients presenting with discordant thyroid function tests – namely, elevated free T4, low free T3, and normal TSH – especially when accompanied by neurological or developmental features such as speech delay and learning difficulties.
Source: Molecular Syndromology
DOI: 10.1159/000551282
Institution: Şişli Etfal Eğitim ve Araştırma Hastanesi
Language: English
Subfield: Nutrition and Dietetics
Field: Nursing
Domain: Health Sciences
Open Access status: green
OpenAlex ID: W7140552102