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. 2025 Sep-Oct;42(5):1076-1077.
doi: 10.1111/pde.15910. Epub 2025 Mar 18.

Multiple Mid-Facial Lesions in an Infant

Miguel Ángel Sánchez-Durán  1 , Antonio Torrelo  1
Affiliations

Multiple Mid-Facial Lesions in an Infant

Miguel Ángel Sánchez-Durán et al. Pediatr Dermatol. 2025 Sep-Oct.
No abstract available

Keywords: KRT17 gene; cysts; genetic dermatosis; pachyonychia congenital; steatocystoma.

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References

    1. S. P. Covello, F. J. Smith, J. H. Sillevis Smitt, et al., “Keratin 17 Mutations Cause Either Steatocystoma Multiplex or Pachyonychia Congenita Type 2,” British Journal of Dermatology 139, no. 3 (1998): 475–480.
    1. V. Fuentelsaz‐del Barrio, V. Parra Blanco, and D. E. Cieza Díaz, “Lesiones Nódulo‐Quísticas Sobre Placa de Alopecia Congénita,” Actas Dermo‐Sifiliográficas 105, no. 1 (2014): 85–86.
    1. J. R. Georgakopoulos, A. Ighani, and J. Yeung, “Numerous Asymptomatic Dermal Cysts: Diagnosis and Treatment of Steatocystoma Multiplex,” Canadian Family Physician 64, no. 12 (2018): 892–899.
    1. E. A. Gordon Spratt, J. Kaplan, R. R. Patel, H. Kamino, and S. M. Ramachandran, “Steatocystoma,” Dermatology Online Journal 19 (2013): 12.
    1. N. J. Wilson, E. A. O'Toole, L. M. Milstone, et al., “The Molecular Genetic Analysis of the Expanding Pachyonychia Congenita Case Collection,” British Journal of Dermatology 171, no. 2 (2014): 343–355.

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