Case Report: A homozygous selenocysteine insertion sequence-binding protein 2 (SECISBP2) gene mutation in a pediatric patient

Selenocysteine insertion sequence-binding protein 2 (SECISBP2) is crucial for the biosynthesis of selenoproteins, including iodothyronine deiodinases, which play a vital role in thyroid hormone metabolism. Mutations in SECISBP2 can disrupt thyroid function, leading to various clinical manifestations...

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Main Authors: Lina Almohammadi, Lama Alsayel, Mohammad Aljumaa, Raghad Alhuthil, Afaf Alsagheir
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-08-01
Series:Frontiers in Pediatrics
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Online Access:https://www.frontiersin.org/articles/10.3389/fped.2025.1637116/full
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author Lina Almohammadi
Lama Alsayel
Mohammad Aljumaa
Raghad Alhuthil
Afaf Alsagheir
Afaf Alsagheir
author_facet Lina Almohammadi
Lama Alsayel
Mohammad Aljumaa
Raghad Alhuthil
Afaf Alsagheir
Afaf Alsagheir
author_sort Lina Almohammadi
collection DOAJ
description Selenocysteine insertion sequence-binding protein 2 (SECISBP2) is crucial for the biosynthesis of selenoproteins, including iodothyronine deiodinases, which play a vital role in thyroid hormone metabolism. Mutations in SECISBP2 can disrupt thyroid function, leading to various clinical manifestations across multiple systems. We present the case of a 3-year-old Saudi female who was referred for genetic testing due to poor growth, developmental abnormalities, and notable facial dysmorphism. Laboratory tests indicated elevated FT4 levels, low T3 levels, and modestly elevated TSH values. Whole-exome sequencing revealed a homozygous pathogenic variant in the SECISBP2 gene (c.358C>T; p.Arg120Ter), correlating with the laboratory findings and the patient's clinical presentation. Additional variants of uncertain significance (VUS) in the ARCN1 and DNA2 genes were also identified but were considered clinically insignificant due to inheritance patterns and the absence of corresponding phenotypes in heterozygous family members. Treatment with liothyronine (L-T3) led to significant clinical improvement in growth and energy levels over a two-year follow-up period. This case highlights the importance of identifying the specific biochemical profile associated with SECISBP2 deficiency and advocates for the inclusion of SECISBP2 in genetic testing panels for endocrine and neurodevelopmental disorders to prevent diagnostic delays. The therapeutic efficacy of liothyronine in such cases is further supported.
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spelling doaj-art-bf83f2a0b952431ab0ff9c971127be542025-08-22T05:26:40ZengFrontiers Media S.A.Frontiers in Pediatrics2296-23602025-08-011310.3389/fped.2025.16371161637116Case Report: A homozygous selenocysteine insertion sequence-binding protein 2 (SECISBP2) gene mutation in a pediatric patientLina Almohammadi0Lama Alsayel1Mohammad Aljumaa2Raghad Alhuthil3Afaf Alsagheir4Afaf Alsagheir5College of Medicine, Alfaisal University, Riyadh, Saudi ArabiaCollege of Medicine, Alfaisal University, Riyadh, Saudi ArabiaCollege of Medicine, Alfaisal University, Riyadh, Saudi ArabiaSection of Pediatric Endocrinology, Department of Pediatrics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi ArabiaCollege of Medicine, Alfaisal University, Riyadh, Saudi ArabiaSection of Pediatric Endocrinology, Department of Pediatrics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi ArabiaSelenocysteine insertion sequence-binding protein 2 (SECISBP2) is crucial for the biosynthesis of selenoproteins, including iodothyronine deiodinases, which play a vital role in thyroid hormone metabolism. Mutations in SECISBP2 can disrupt thyroid function, leading to various clinical manifestations across multiple systems. We present the case of a 3-year-old Saudi female who was referred for genetic testing due to poor growth, developmental abnormalities, and notable facial dysmorphism. Laboratory tests indicated elevated FT4 levels, low T3 levels, and modestly elevated TSH values. Whole-exome sequencing revealed a homozygous pathogenic variant in the SECISBP2 gene (c.358C>T; p.Arg120Ter), correlating with the laboratory findings and the patient's clinical presentation. Additional variants of uncertain significance (VUS) in the ARCN1 and DNA2 genes were also identified but were considered clinically insignificant due to inheritance patterns and the absence of corresponding phenotypes in heterozygous family members. Treatment with liothyronine (L-T3) led to significant clinical improvement in growth and energy levels over a two-year follow-up period. This case highlights the importance of identifying the specific biochemical profile associated with SECISBP2 deficiency and advocates for the inclusion of SECISBP2 in genetic testing panels for endocrine and neurodevelopmental disorders to prevent diagnostic delays. The therapeutic efficacy of liothyronine in such cases is further supported.https://www.frontiersin.org/articles/10.3389/fped.2025.1637116/fullSECISBP2 genethyroid functiondysmorphic featuresshort statureSaudi Arabia
spellingShingle Lina Almohammadi
Lama Alsayel
Mohammad Aljumaa
Raghad Alhuthil
Afaf Alsagheir
Afaf Alsagheir
Case Report: A homozygous selenocysteine insertion sequence-binding protein 2 (SECISBP2) gene mutation in a pediatric patient
Frontiers in Pediatrics
SECISBP2 gene
thyroid function
dysmorphic features
short stature
Saudi Arabia
title Case Report: A homozygous selenocysteine insertion sequence-binding protein 2 (SECISBP2) gene mutation in a pediatric patient
title_full Case Report: A homozygous selenocysteine insertion sequence-binding protein 2 (SECISBP2) gene mutation in a pediatric patient
title_fullStr Case Report: A homozygous selenocysteine insertion sequence-binding protein 2 (SECISBP2) gene mutation in a pediatric patient
title_full_unstemmed Case Report: A homozygous selenocysteine insertion sequence-binding protein 2 (SECISBP2) gene mutation in a pediatric patient
title_short Case Report: A homozygous selenocysteine insertion sequence-binding protein 2 (SECISBP2) gene mutation in a pediatric patient
title_sort case report a homozygous selenocysteine insertion sequence binding protein 2 secisbp2 gene mutation in a pediatric patient
topic SECISBP2 gene
thyroid function
dysmorphic features
short stature
Saudi Arabia
url https://www.frontiersin.org/articles/10.3389/fped.2025.1637116/full
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