# Permanent Congenital Hypothyroidism due to Rare Thyroglobulin Gene Variant (p.Cys1476Arg): A Delayed Diagnosis of Thyroid Dyshormonogenesis

**Authors:** Ghassan Mohamadsalih, Khalid Al Bureshad, Idris Mohammed, Shiga Chirayath, Elwaseila Hamdoun, Khalid Hussain

PMC · DOI: 10.1155/carm/5313611 · Case Reports in Medicine · 2025-05-24

## TL;DR

A Qatari boy with congenital hypothyroidism was diagnosed with a rare thyroglobulin gene mutation causing thyroid hormone production issues.

## Contribution

Reports a rare thyroglobulin gene variant (p.Cys1476Arg) in a Qatari patient with delayed diagnosis of thyroid dyshormonogenesis.

## Key findings

- A 10.5-year-old boy was found to have a homozygous thyroglobulin gene variant (p.Cys1476Arg) causing congenital hypothyroidism.
- The variant had been previously reported in only five other patients in the Middle East.
- Delayed diagnosis highlights the importance of determining the underlying cause of congenital hypothyroidism for proper management.

## Abstract

Thyroid dyshormonogenesis is an inherited hypothyroidism caused by a monogenic defect, in the vast majority of cases, in thyroid hormone biosynthesis. It is commonly associated with thyroid enlargement which is vulnerable to nodule formation. We present a Qatari patient with an overlooked diagnosis of thyroid dyshormonogenesis due to thyroglobulin gene mutation. A 10.5-year-old boy has been following up for congenital hypothyroidism since the age of 4 years. He was diagnosed by newborn screening that was confirmed by laboratory thyroid function testing; however, no further workup was done to understand the underlying cause. He was born to consanguineous parents with a family history of hypothyroidism. The patient was not adherent to his medication and follow-up visits, and thyroid-stimulating hormone was above 5 mIU/L most of the time. On examination, he had a goiter that developed a few months ago. The father admitted that it was there at birth but disappeared with levothyroxine therapy. Molecular genetics revealed a homozygous c.4426T > C, p.Cys1476Arg variant in the thyroglobulin gene. This variant was only previously reported, in the Middle East region, in five patients. Determination of congenital hypothyroidism underlying etiology is important for family counseling and long-term management.

## Linked entities

- **Diseases:** congenital hypothyroidism (MONDO:0018612), thyroid dyshormonogenesis (MONDO:0010132)

## Full-text entities

- **Genes:** TG (thyroglobulin) [NCBI Gene 7038] {aka AITD3, TGN}
- **Diseases:** Congenital Hypothyroidism (MESH:D003409), hypothyroidism (MESH:D007037), Thyroid Dyshormonogenesis (MESH:C564766), goiter (MESH:D006042)
- **Chemicals:** levothyroxine (MESH:D013974)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** c.4426T > C, p.Cys1476Arg

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12126254/full.md

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12126254/full.md

## References

16 references — full list in the complete paper: https://tomesphere.com/paper/PMC12126254/full.md

---
Source: https://tomesphere.com/paper/PMC12126254