A spectrum of mutations in keratins K6a, K16 and K17 causing pachyonychia congenita

Haihui Liao, Jane M. Sayers, Neil J. Wilson, Alan D. Irvine, Jemima E. Mellerio, Eulalia Baselga, Susan J. Bayliss, Vera Uliana, Michele Fimiani, E. Birgitte Lane, W. H Irwin McLean, Sancy Leachman, Frances J D Smith

Research output: Contribution to journalArticle

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Abstract

Background: Pachyonychia congenita (PC) is a rare autosomal dominant keratin disorder, subdivided into two major variants, PC-1 and PC-2. Predominant characteristics include hypertrophic nail dystrophy, focal palmoplantar keratoderma and oral leukokeratosis. Multiple steatocystomas that develop during puberty are a useful feature distinguishing PC-2 from PC-1. At the molecular level it has been shown that mutations in keratin K6a or K16 cause PC-1 whereas those in K6b or K17 lead to PC-2. Objective: To identify mutations in 22 families presenting with clinical symptoms of either PC-1/focal non-epidermolytic palmoplantar keratoderma (FNEPPK) or PC-2. Methods: Mutation analysis was performed on genomic DNA from PC patients by direct sequencing. Results: Here, we report four new missense and five known mutations in K6a; one new deletion and three previously identified missense mutations in K16; plus one known mutation in K17. Conclusion: With one exception, all these heterozygous mutations are within the highly conserved helix boundary motif regions at either end of the keratin rod domain. In one sporadic case, a unique mutation in K16 resulting in deletion of 24 bp was found within the central rod domain, in a child with a phenotype predominantly consisting of focal plantar keratoderma. The identification of mutations in cases of PC is prerequisite for future development of gene-specific and/or mutation-specific therapies.

Original languageEnglish (US)
Pages (from-to)199-205
Number of pages7
JournalJournal of Dermatological Science
Volume48
Issue number3
DOIs
StatePublished - Dec 2007
Externally publishedYes

Fingerprint

Pachyonychia Congenita
Keratins
Mutation
Nails
Genes
DNA
Oral Leukoplakia
Missense Mutation
Puberty

Keywords

  • Bullous disease
  • Genodermatosis
  • Keratinizing disorder
  • Keratoderma
  • Nail dystrophy

ASJC Scopus subject areas

  • Dermatology

Cite this

Liao, H., Sayers, J. M., Wilson, N. J., Irvine, A. D., Mellerio, J. E., Baselga, E., ... Smith, F. J. D. (2007). A spectrum of mutations in keratins K6a, K16 and K17 causing pachyonychia congenita. Journal of Dermatological Science, 48(3), 199-205. https://doi.org/10.1016/j.jdermsci.2007.07.003

A spectrum of mutations in keratins K6a, K16 and K17 causing pachyonychia congenita. / Liao, Haihui; Sayers, Jane M.; Wilson, Neil J.; Irvine, Alan D.; Mellerio, Jemima E.; Baselga, Eulalia; Bayliss, Susan J.; Uliana, Vera; Fimiani, Michele; Lane, E. Birgitte; McLean, W. H Irwin; Leachman, Sancy; Smith, Frances J D.

In: Journal of Dermatological Science, Vol. 48, No. 3, 12.2007, p. 199-205.

Research output: Contribution to journalArticle

Liao, H, Sayers, JM, Wilson, NJ, Irvine, AD, Mellerio, JE, Baselga, E, Bayliss, SJ, Uliana, V, Fimiani, M, Lane, EB, McLean, WHI, Leachman, S & Smith, FJD 2007, 'A spectrum of mutations in keratins K6a, K16 and K17 causing pachyonychia congenita', Journal of Dermatological Science, vol. 48, no. 3, pp. 199-205. https://doi.org/10.1016/j.jdermsci.2007.07.003
Liao, Haihui ; Sayers, Jane M. ; Wilson, Neil J. ; Irvine, Alan D. ; Mellerio, Jemima E. ; Baselga, Eulalia ; Bayliss, Susan J. ; Uliana, Vera ; Fimiani, Michele ; Lane, E. Birgitte ; McLean, W. H Irwin ; Leachman, Sancy ; Smith, Frances J D. / A spectrum of mutations in keratins K6a, K16 and K17 causing pachyonychia congenita. In: Journal of Dermatological Science. 2007 ; Vol. 48, No. 3. pp. 199-205.
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abstract = "Background: Pachyonychia congenita (PC) is a rare autosomal dominant keratin disorder, subdivided into two major variants, PC-1 and PC-2. Predominant characteristics include hypertrophic nail dystrophy, focal palmoplantar keratoderma and oral leukokeratosis. Multiple steatocystomas that develop during puberty are a useful feature distinguishing PC-2 from PC-1. At the molecular level it has been shown that mutations in keratin K6a or K16 cause PC-1 whereas those in K6b or K17 lead to PC-2. Objective: To identify mutations in 22 families presenting with clinical symptoms of either PC-1/focal non-epidermolytic palmoplantar keratoderma (FNEPPK) or PC-2. Methods: Mutation analysis was performed on genomic DNA from PC patients by direct sequencing. Results: Here, we report four new missense and five known mutations in K6a; one new deletion and three previously identified missense mutations in K16; plus one known mutation in K17. Conclusion: With one exception, all these heterozygous mutations are within the highly conserved helix boundary motif regions at either end of the keratin rod domain. In one sporadic case, a unique mutation in K16 resulting in deletion of 24 bp was found within the central rod domain, in a child with a phenotype predominantly consisting of focal plantar keratoderma. The identification of mutations in cases of PC is prerequisite for future development of gene-specific and/or mutation-specific therapies.",
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T1 - A spectrum of mutations in keratins K6a, K16 and K17 causing pachyonychia congenita

AU - Liao, Haihui

AU - Sayers, Jane M.

AU - Wilson, Neil J.

AU - Irvine, Alan D.

AU - Mellerio, Jemima E.

AU - Baselga, Eulalia

AU - Bayliss, Susan J.

AU - Uliana, Vera

AU - Fimiani, Michele

AU - Lane, E. Birgitte

AU - McLean, W. H Irwin

AU - Leachman, Sancy

AU - Smith, Frances J D

PY - 2007/12

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N2 - Background: Pachyonychia congenita (PC) is a rare autosomal dominant keratin disorder, subdivided into two major variants, PC-1 and PC-2. Predominant characteristics include hypertrophic nail dystrophy, focal palmoplantar keratoderma and oral leukokeratosis. Multiple steatocystomas that develop during puberty are a useful feature distinguishing PC-2 from PC-1. At the molecular level it has been shown that mutations in keratin K6a or K16 cause PC-1 whereas those in K6b or K17 lead to PC-2. Objective: To identify mutations in 22 families presenting with clinical symptoms of either PC-1/focal non-epidermolytic palmoplantar keratoderma (FNEPPK) or PC-2. Methods: Mutation analysis was performed on genomic DNA from PC patients by direct sequencing. Results: Here, we report four new missense and five known mutations in K6a; one new deletion and three previously identified missense mutations in K16; plus one known mutation in K17. Conclusion: With one exception, all these heterozygous mutations are within the highly conserved helix boundary motif regions at either end of the keratin rod domain. In one sporadic case, a unique mutation in K16 resulting in deletion of 24 bp was found within the central rod domain, in a child with a phenotype predominantly consisting of focal plantar keratoderma. The identification of mutations in cases of PC is prerequisite for future development of gene-specific and/or mutation-specific therapies.

AB - Background: Pachyonychia congenita (PC) is a rare autosomal dominant keratin disorder, subdivided into two major variants, PC-1 and PC-2. Predominant characteristics include hypertrophic nail dystrophy, focal palmoplantar keratoderma and oral leukokeratosis. Multiple steatocystomas that develop during puberty are a useful feature distinguishing PC-2 from PC-1. At the molecular level it has been shown that mutations in keratin K6a or K16 cause PC-1 whereas those in K6b or K17 lead to PC-2. Objective: To identify mutations in 22 families presenting with clinical symptoms of either PC-1/focal non-epidermolytic palmoplantar keratoderma (FNEPPK) or PC-2. Methods: Mutation analysis was performed on genomic DNA from PC patients by direct sequencing. Results: Here, we report four new missense and five known mutations in K6a; one new deletion and three previously identified missense mutations in K16; plus one known mutation in K17. Conclusion: With one exception, all these heterozygous mutations are within the highly conserved helix boundary motif regions at either end of the keratin rod domain. In one sporadic case, a unique mutation in K16 resulting in deletion of 24 bp was found within the central rod domain, in a child with a phenotype predominantly consisting of focal plantar keratoderma. The identification of mutations in cases of PC is prerequisite for future development of gene-specific and/or mutation-specific therapies.

KW - Bullous disease

KW - Genodermatosis

KW - Keratinizing disorder

KW - Keratoderma

KW - Nail dystrophy

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