Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1984 1
1998 1
1999 1
2000 1
2001 1
2004 1
2007 1
2009 1
2010 2
2011 2
2012 4
2013 3
2014 4
2015 3
2017 1
2018 1
2019 3
2020 3
2022 1
2023 1
2024 1

Text availability

Article attribute

Article type

Publication date

Search Results

31 results

Results by year

Filters applied: . Clear all
Quoted phrase not found in phrase index: "Pachyonychia congenita 3"
Page 1
Pachyonychia Congenita.
Tan Y, Ma DL. Tan Y, et al. Indian J Pediatr. 2024 Mar;91(3):300-301. doi: 10.1007/s12098-023-04567-z. Epub 2023 Jun 8. Indian J Pediatr. 2024. PMID: 37289311 No abstract available.
Coexistence of pachyonychia congenita and hidradenitis suppurativa: more than a coincidence.
Pavlovsky M, Peled A, Sarig O, Astman N, Malki L, Meijers O, Assaf S, Schwartz J, Malovitski K, Hansen D, Sprecher E, Samuelov L. Pavlovsky M, et al. Br J Dermatol. 2022 Sep;187(3):392-400. doi: 10.1111/bjd.21674. Epub 2022 Jun 17. Br J Dermatol. 2022. PMID: 35606927 Free PMC article.
BACKGROUND: The coexistence of pachyonychia congenita (PC) and hidradenitis suppurativa (HS) has been described in case reports. ...What is already known about this topic? The coexistence of pachyonychia congenita (PC) and hidradenitis suppurativa (HS) …
BACKGROUND: The coexistence of pachyonychia congenita (PC) and hidradenitis suppurativa (HS) has been described in case report …
Symptomatic mucosal involvement in pachyonychia congenita: challenges in infants and young children.
Goldberg I, Mashiah J, Kutz A, Derowe A, Warshauer E, Schwartz ME, Smith F, Sprecher E, Hansen CD. Goldberg I, et al. Br J Dermatol. 2020 Mar;182(3):708-713. doi: 10.1111/bjd.18742. Epub 2019 Dec 25. Br J Dermatol. 2020. PMID: 31777952
BACKGROUND: Pachyonychia congenita (PC) is a rare autosomal dominant genodermatosis caused by a mutation in any one of five keratin genes (KRT6A, KRT6B, KRT6C, KRT16 or KRT17). ...Usually simple feeding solutions may prevent complications and failure to thrive. What …
BACKGROUND: Pachyonychia congenita (PC) is a rare autosomal dominant genodermatosis caused by a mutation in any one of five ke …
Pachyonychia congenita in pediatric patients: natural history, features, and impact.
Shah S, Boen M, Kenner-Bell B, Schwartz M, Rademaker A, Paller AS. Shah S, et al. JAMA Dermatol. 2014 Feb;150(2):146-53. doi: 10.1001/jamadermatol.2013.6448. JAMA Dermatol. 2014. PMID: 24132595
IMPORTANCE Nail dystrophy in early childhood often suggests a diagnosis of pachyonychia congenita (PC). No previous investigation has focused on the early signs of PC and the natural course of the disease. ...EXPOSURE Individuals with pachyonychia congenit …
IMPORTANCE Nail dystrophy in early childhood often suggests a diagnosis of pachyonychia congenita (PC). No previous investigat …
Revisiting pachyonychia congenita: a case-cohort study of 815 patients.
Samuelov L, Smith FJD, Hansen CD, Sprecher E. Samuelov L, et al. Br J Dermatol. 2020 Mar;182(3):738-746. doi: 10.1111/bjd.18794. Epub 2020 Jan 14. Br J Dermatol. 2020. PMID: 31823354
BACKGROUND: Pachyonychia congenita (PC) is a group of autosomal dominant disorders caused by mutations in one of five keratin genes (KRT6A, KRT6B, KRT6C, KRT16, KRT17). ...METHODS: In total, 815 individuals with confirmed keratin mutations registered in the Internat …
BACKGROUND: Pachyonychia congenita (PC) is a group of autosomal dominant disorders caused by mutations in one of five keratin …
Olmsted syndrome: clinical, molecular and therapeutic aspects.
Duchatelet S, Hovnanian A. Duchatelet S, et al. Orphanet J Rare Dis. 2015 Mar 17;10:33. doi: 10.1186/s13023-015-0246-5. Orphanet J Rare Dis. 2015. PMID: 25886873 Free PMC article. Review.
Most of reported OS cases are sporadic, although familial cases with different mode of inheritance were also described. Mutations in TRPV3 (Transient receptor potential vanilloid-3) gene have recently been identified as a cause of autosomal dominant (gain-of-function mutat …
Most of reported OS cases are sporadic, although familial cases with different mode of inheritance were also described. Mutations in TRPV3 ( …
Pachyonychia congenita tarda.
Hannaford RS, Stapleton K. Hannaford RS, et al. Australas J Dermatol. 2000 Aug;41(3):175-7. doi: 10.1046/j.1440-0960.2000.00425.x. Australas J Dermatol. 2000. PMID: 10954990 Review.
His sister has overcurvature of the fifth toenails. A diagnosis of pachyonychia congenita tarda was made. His case is compared with 14 other reported cases of this rare syndrome....
His sister has overcurvature of the fifth toenails. A diagnosis of pachyonychia congenita tarda was made. His case is compared …
Hidradenitis suppurrativa (acne inversa) as a systemic disease.
Dessinioti C, Katsambas A, Antoniou C. Dessinioti C, et al. Clin Dermatol. 2014 May-Jun;32(3):397-408. doi: 10.1016/j.clindermatol.2013.11.006. Epub 2013 Nov 22. Clin Dermatol. 2014. PMID: 24767187 Review.
There are several reports in the literature of the coexistence of HS with other diseases, including pyoderma gangrenosum, PASH syndrome, Adamantiades-Behcet's disease, spondylarthropathy, Crohn's disease, SAPHO, pachyonychia congenita, Dowling-Degos disease, and the …
There are several reports in the literature of the coexistence of HS with other diseases, including pyoderma gangrenosum, PASH syndrome, Ada …
Eruptive vellus hair cysts: a systematic review.
Torchia D, Vega J, Schachner LA. Torchia D, et al. Am J Clin Dermatol. 2012 Feb 1;13(1):19-28. doi: 10.2165/11589050-000000000-00000. Am J Clin Dermatol. 2012. PMID: 21958358 Review.
EVHC may be present at birth and may appear at any age, although they show a clear trend towards occurring during the first 3 decades of life. A strong clue to the heavy influence of genes on the occurrence of EVHC is provided by the numerous reports of families in whom tw …
EVHC may be present at birth and may appear at any age, although they show a clear trend towards occurring during the first 3 decades …
31 results