# Case Report: Hydroxychloroquine in an infant with NKX2-1-associated interstitial lung disease

**Authors:** Di Qing, Xuehua Xu, Tingting Shi, Huifeng Fan, Dongwei Zhang, Diyuan Yang, Gen Lu

PMC · DOI: 10.3389/fped.2025.1619722 · Frontiers in Pediatrics · 2025-10-16

## TL;DR

A 7-month-old infant with a rare genetic disorder showed reduced oxygen needs after being treated with hydroxychloroquine for lung disease.

## Contribution

This case report explores the potential use of hydroxychloroquine in treating NKX2-1-associated interstitial lung disease.

## Key findings

- The infant's oxygen demand decreased after hydroxychloroquine treatment.
- A pathogenic variant in the NKX2-1 gene was identified through whole-exome sequencing.
- The patient required mechanical ventilation and showed developmental delays.

## Abstract

This study presents a case of brain–lung–thyroid syndrome caused by a pathogenic variant in the NKX2-1 gene, which is characterized by interstitial lung disease. A 7-month-old female infant was hospitalized for over half a month for cyanosis. The full-term infant developed respiratory distress syndrome soon after delivery, requiring mechanical ventilation, and was diagnosed with congenital hypothyroidism. In the first seven months of life, the infant also showed hypotonia, feeding difficulties, and developmental delays. Chest CT findings demonstrated generalized ground-glass opacities in both lung fields. A heterozygous pathogenic variant of the NKX2-1 gene [NM_001079668.3:c.583C>T (p.Arg195Trp)] was identified by whole-exome sequencing. The infant received a combination therapy, comprising supplementary thyroxine, nutritional support, high-flow nasal cannula oxygen therapy, and exploratory treatment with hydroxychloroquine. High-flow nasal cannula oxygen therapy was administered after discharge. The patient was followed up for over 2 months, and the patient had changed to low-flow oxygen therapy, although she developed radiographic progression. Studies on hydroxychloroquine for the treatment of interstitial lung diseases are limited. This article describes a case of interstitial lung disease caused by a pathogenic variant in the NKX2-1 gene, whose oxygen demand decreased after treatment with hydroxychloroquine.

## Linked entities

- **Genes:** NKX2-1 (NK2 homeobox 1) [NCBI Gene 7080]
- **Chemicals:** hydroxychloroquine (PubChem CID 3652), thyroxine (PubChem CID 853)
- **Diseases:** brain–lung–thyroid syndrome (MONDO:0012593), interstitial lung disease (MONDO:0015925), congenital hypothyroidism (MONDO:0018612), respiratory distress syndrome (MONDO:0009971)

## Full-text entities

- **Genes:** NKX2-1 (NK2 homeobox 1) [NCBI Gene 7080] {aka BCH, BHC, NK-2, NKX2.1, NKX2A, NMTC1}
- **Diseases:** developmental delays (MESH:D002658), cyanosis (MESH:D003490), opacities (MESH:D003318), interstitial lung disease (MESH:D017563), hypotonia (MESH:D009123), respiratory distress syndrome (MESH:D012128), brain-lung-thyroid syndrome (MESH:C567034), congenital hypothyroidism (MESH:D003409)
- **Chemicals:** Hydroxychloroquine (MESH:D006886), thyroxine (MESH:D013974), oxygen (MESH:D010100)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** p.Arg195Trp, c.583C>T

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12571818/full.md

## References

25 references — full list in the complete paper: https://tomesphere.com/paper/PMC12571818/full.md

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Source: https://tomesphere.com/paper/PMC12571818