# Connexin 30 (GJB6) deletion as a cause of a false positive sweat test result

**Authors:** Anna Rossell, Aleix Soler-Garcia, Loreto Martorell, Maria Antònia Claveria, Laura Valero, Sílvia Rodríguez, Cèlia Badenas, Maria Cols-Roig

PMC · DOI: 10.1007/s00431-025-06220-7 · European Journal of Pediatrics · 2025-06-12

## TL;DR

This study identifies a genetic mutation in connexin 30 as a new cause of false positive sweat test results, which could lead to misdiagnosis of cystic fibrosis.

## Contribution

The study reports a previously unreported cause of false positive sweat tests linked to homozygous connexin 30 gene mutations.

## Key findings

- Three patients with homozygous connexin 30 deletions had abnormal sweat test results.
- Two patients with the mutation experienced severe hyponatremic dehydration.
- No other mutation patterns were associated with positive sweat tests in the study.

## Abstract

The sweat test (ST) is the gold standard for the diagnosis of cystic fibrosis. There are several reports in the literature regarding conditions that are known to be associated with a false positive result. The aim of this article is to describe a previously unreported cause of a false positive ST. An observational, cross-sectional single-center study was performed. We recruited three patients with a neurosensory deafness caused by a deletion in both alleles of connexin 30. The first-degree relatives of these three patients with hearing impairment due to other mutations were also included. A ST was performed in all the selected cases. Among the three patients with a deletion in both connexin 30 alleles, two had a positive ST, whereas the third patient had a close-to-positivity borderline result (57 mmol/L). Moreover, there were no positive sweat tests in individuals with other mutation patterns.

Conclusion: Patients with affection of both alleles of connexin 30 were the only ones to show a positive ST, which may translate to a higher risk of hyponatremic dehydration. The reason for the ST positivity remains unclear and may be related to the fact that connexin 30 plays a role in modulating other molecules in both the inner ear and sweat glands.
What is Known:• The sweat test is the gold standard for the diagnosis of cystic fibrosis. However, the causes of false positives in the test are increasingly recognized.What is New:• This study describes a previously unreported cause of a false positive sweat test. Three patients with homozygous mutations in the connexin 30 gene are described. All of them had an abnormal sweat test, and two of them presented with severe hyponatremic dehydration.

What is Known:

• The sweat test is the gold standard for the diagnosis of cystic fibrosis. However, the causes of false positives in the test are increasingly recognized.

What is New:

• This study describes a previously unreported cause of a false positive sweat test. Three patients with homozygous mutations in the connexin 30 gene are described. All of them had an abnormal sweat test, and two of them presented with severe hyponatremic dehydration.

## Linked entities

- **Genes:** gjb1 (gap junction protein beta 1) [NCBI Gene 407921], GJB6 (gap junction protein beta 6) [NCBI Gene 10804]
- **Diseases:** cystic fibrosis (MONDO:0009061)

## Full-text entities

- **Genes:** GJB6 (gap junction protein beta 6) [NCBI Gene 10804] {aka CX30, DFNA3, DFNA3B, DFNB1B, ECTD2, ED2}
- **Diseases:** neurosensory deafness (MESH:D006319), cystic fibrosis (MESH:D003550), hearing impairment (MESH:D034381), hyponatremic dehydration (MESH:D003681)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12162805/full.md

## References

8 references — full list in the complete paper: https://tomesphere.com/paper/PMC12162805/full.md

---
Source: https://tomesphere.com/paper/PMC12162805