# Correction: Case Report: Autosomal recessive palmoplantar keratoderma with additional bilateral hearing loss due to a pathogenic frameshift deletion in FAM83G

**Authors:** Mónica Mora-Gómez, Marta Feito, Natalia Gallego-Zazo, Rocío Maseda-Pedrero, Tristán G. Sobral-Costas, Lucía Miranda-Alcaraz, Valeria Vásquez-Amell, Manuel Rodríguez-Canó, Alejandro Parra, Mario Cazalla, Pedro Arias, Cristina Silván, Juan A. Jiménez-Estrada, Víctor L. Ruiz-Pérez, Julián Nevado, Pablo Lapunzina, Jair Tenorio-Castano

PMC · DOI: 10.3389/fmed.2026.1779531 · Frontiers in Medicine · 2026-02-13

## Full-text entities

- **Genes:** SACK1G (scaffolding CK1 anchoring protein G) [NCBI Gene 644815] {aka FAM83G, PAWS1}
- **Diseases:** palmoplantar keratoderma (MESH:D007645), hearing loss (MESH:D034381)

## Full text

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Source: https://tomesphere.com/paper/PMC12947843