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Year Number of Results
1984 1
1988 2
1989 1
1990 1
1991 1
1996 2
1999 2
2000 1
2001 1
2003 1
2005 7
2006 1
2007 1
2008 2
2010 3
2011 3
2012 4
2013 3
2014 4
2015 4
2016 3
2017 2
2018 3
2019 5
2020 1
2021 2
2023 2
2024 1

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57 results

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Page 1
Pediatric Nail Disorders.
Bellet JS. Bellet JS. Dermatol Clin. 2021 Apr;39(2):231-243. doi: 10.1016/j.det.2020.12.005. Epub 2021 Feb 10. Dermatol Clin. 2021. PMID: 33745636 Review.
Pachyonychia congenita.
Feinstein A, Friedman J, Schewach-Millet M. Feinstein A, et al. J Am Acad Dermatol. 1988 Oct;19(4):705-11. doi: 10.1016/s0190-9622(88)70226-1. J Am Acad Dermatol. 1988. PMID: 3053803 Review.
Pachyonychia congenita is a rare hereditary disorder characterized mainly by nail hypertrophy and dyskeratoses of skin and mucous membranes. A thorough literature survey since its first description in 1904 up to 1985 revealed 168 cases of pachyonychia cong
Pachyonychia congenita is a rare hereditary disorder characterized mainly by nail hypertrophy and dyskeratoses of skin and muc
New described dermatological disorders.
Gönül M, Cevirgen Cemil B, Keseroglu HO, Kaya Akis H. Gönül M, et al. Biomed Res Int. 2014;2014:616973. doi: 10.1155/2014/616973. Epub 2014 Aug 28. Biomed Res Int. 2014. PMID: 25243162 Free PMC article. Review.
Syndromes included are "circumferential skin creases Kunze type" and "unusual type of pachyonychia congenita or a new syndrome"; autoinflammatory diseases include "chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature (CANDLE) syndrome …
Syndromes included are "circumferential skin creases Kunze type" and "unusual type of pachyonychia congenita or a new syndrome …
Keratins and skin disease.
Knöbel M, O'Toole EA, Smith FJ. Knöbel M, et al. Cell Tissue Res. 2015 Jun;360(3):583-9. doi: 10.1007/s00441-014-2105-4. Epub 2015 Jan 27. Cell Tissue Res. 2015. PMID: 25620412 Review.
Cutaneous disorders include epidermolysis bullosa simplex, palmoplantar keratoderma, epidermolytic ichthyosis and pachyonychia congenita. Both clinical and laboratory observations confirm a major role for keratins in maintaining epidermal cell-cell adhesion. ...
Cutaneous disorders include epidermolysis bullosa simplex, palmoplantar keratoderma, epidermolytic ichthyosis and pachyonychia con
Posttranslational modifications of keratins and their associated proteins as therapeutic targets in keratin diseases.
Li P, Rietscher K, Jopp H, Magin TM, Omary MB. Li P, et al. Curr Opin Cell Biol. 2023 Dec;85:102264. doi: 10.1016/j.ceb.2023.102264. Epub 2023 Nov 3. Curr Opin Cell Biol. 2023. PMID: 37925932 Review.
Keratin gene mutations cause multiple rare monoallelic epithelial diseases termed keratinopathies, including the skin diseases Epidermolysis Bullosa Simplex (EBS) and Pachyonychia Congenita (PC), with limited available therapies. The disease-related keratin mutation …
Keratin gene mutations cause multiple rare monoallelic epithelial diseases termed keratinopathies, including the skin diseases Epidermolysis …
The phenotypic and molecular genetic features of pachyonychia congenita.
McLean WH, Hansen CD, Eliason MJ, Smith FJ. McLean WH, et al. J Invest Dermatol. 2011 May;131(5):1015-7. doi: 10.1038/jid.2011.59. Epub 2011 Mar 24. J Invest Dermatol. 2011. PMID: 21430705 Free article. Review.
Pachyonychia congenita (PC) is an autosomal dominant genodermatosis caused by heterozygous mutations in any one of the genes encoding the differentiation-specific keratins K6a, K6b, K16, or K17. ...
Pachyonychia congenita (PC) is an autosomal dominant genodermatosis caused by heterozygous mutations in any one of the genes e
Keratin 17 in disease pathogenesis: from cancer to dermatoses.
Yang L, Zhang S, Wang G. Yang L, et al. J Pathol. 2019 Feb;247(2):158-165. doi: 10.1002/path.5178. Epub 2018 Dec 7. J Pathol. 2019. PMID: 30306595 Review.
Moreover, genetic mutation in KRT17 is related to tissue-specific diseases, represented by steatocystoma multiplex and pachyonychia congenita. In this review, we summarize our findings concerning the regulatory mechanisms of K17 overexpression in psoriasis and compa …
Moreover, genetic mutation in KRT17 is related to tissue-specific diseases, represented by steatocystoma multiplex and pachyonychia
Treatment of pachyonychia congenita.
Milstone LM, Fleckman P, Leachman SA, Leigh IM, Paller AS, van Steensel MA, Swartling C. Milstone LM, et al. J Investig Dermatol Symp Proc. 2005 Oct;10(1):18-20. doi: 10.1111/j.1087-0024.2005.10203.x. J Investig Dermatol Symp Proc. 2005. PMID: 16250205 Free article. Review.
There are currently no specific treatments for pachyonychia congenita (PC). Available treatments generally are directed at specific manifestations of the disorder, and an effective treatment plan must recognize that different patients are more or less troubled by di …
There are currently no specific treatments for pachyonychia congenita (PC). Available treatments generally are directed at spe …
A KRT16 mutation in the first Chinese pedigree with Pachyonychia congenita and review of the literatures.
Xu Q, Zhang Q, Tang L, Jin L, Wang X, Kan L, Zheng X, Yang S. Xu Q, et al. J Cosmet Dermatol. 2019 Dec;18(6):1930-1934. doi: 10.1111/jocd.12905. Epub 2019 Mar 12. J Cosmet Dermatol. 2019. PMID: 30859684 Review.
BACKGROUND: Pachyonychia congenita (PC), a rare autosomal dominant disorder, is featured by significant hypertrophic nail, palmoplantar keratoderma, and plantar pain. ...
BACKGROUND: Pachyonychia congenita (PC), a rare autosomal dominant disorder, is featured by significant hypertrophic nail, pal …
Management of Plantar Keratodermas(Lessons from Pachyonychia Congenita).
Porter RM, Bravo AA, Smith FJD. Porter RM, et al. J Am Podiatr Med Assoc. 2017 Sep;107(5):428-435. doi: 10.7547/16-043. J Am Podiatr Med Assoc. 2017. PMID: 29077501 Review.
This review focuses on the rare autosomal dominant keratin disorder pachyonychia congenita, which presents with particularly painful plantar keratoderma for which there is no specific treatment. ...This finding has stimulated a drive for alternative treatment option …
This review focuses on the rare autosomal dominant keratin disorder pachyonychia congenita, which presents with particularly p …
57 results