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CORRECTION article

Front. Med., 13 February 2026

Sec. Dermatology

Volume 13 - 2026 | https://doi.org/10.3389/fmed.2026.1779531

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

    MM

    Mónica Mora-Gómez 1,2,3

    MF

    Marta Feito 4

    NG

    Natalia Gallego-Zazo 1,2,3

    RM

    Rocío Maseda-Pedrero 4

    TG

    Tristán G. Sobral-Costas 4

    LM

    Lucía Miranda-Alcaraz 1,2,3

    VV

    Valeria Vásquez-Amell 1,2,3

    MR

    Manuel Rodríguez-Canó 1,2,3

    AP

    Alejandro Parra 1,2,3

    MC

    Mario Cazalla 1,2,3

    PA

    Pedro Arias 1,2,3

    CS

    Cristina Silván 1,2,3

    JA

    Juan A. Jiménez-Estrada 1,2,3

    VL

    Víctor L. Ruiz-Pérez 1,2,3,5

    JN

    Julián Nevado 1,2,3

    PL

    Pablo Lapunzina 1,2,3

    JT

    Jair Tenorio-Castano 1,2,3*

  • 1. CIBERER, Centro de Investigación Biomédica en Red de Enfermedades Raras, Madrid, Spain

  • 2. INGEMM-IdIPAZ, Institute of Medical and Molecular Genetics, La Paz University Hospital, Madrid, Spain

  • 3. ITHACA, European Reference Network, Brussels, Belgium

  • 4. Dermatology Unit, La Paz University Hospital, Madrid, Spain

  • 5. Instituto de Investigaciones Biomedicas Sols-Morreale (IIBM), CSIC-UAM, Madrid, Spain

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An incorrect Funding statement was provided. The funding information was incomplete. The correct funding statement reads:

“The author(s) declared that financial support was received for this work and/or its publication. This study has been funded by Instituto de Salud Carlos III through the projects PMP21/00063 and PMP22/00049 and by Next Generation EU funds, which finance the actions of the Recovery and Resilience Facility (RRF).”

The original version of this article has been updated.

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Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Summary

Keywords

palmoplantar keratoderma, FAM83G , genodermatosis, skin disorder, bilateral hearing loss, genomic medicine, massive paralleled sequencing

Citation

Mora-Gómez M, Feito M, Gallego-Zazo N, Maseda-Pedrero R, Sobral-Costas TG, Miranda-Alcaraz L, Vásquez-Amell V, Rodríguez-Canó M, Parra A, Cazalla M, Arias P, Silván C, Jiménez-Estrada JA, Ruiz-Pérez VL, Nevado J, Lapunzina P and Tenorio-Castano J (2026) Correction: Case Report: Autosomal recessive palmoplantar keratoderma with additional bilateral hearing loss due to a pathogenic frameshift deletion in FAM83G. Front. Med. 13:1779531. doi: 10.3389/fmed.2026.1779531

Received

02 January 2026

Revised

27 January 2026

Accepted

28 January 2026

Published

13 February 2026

Approved by

Frontiers Editorial Office, Frontiers Media SA, Switzerland

Volume

13 - 2026

Updates

Copyright

*Correspondence: Jair Tenorio-Castano, ;

Disclaimer

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

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