Pachyonychia congenita tarda

Pachyonychia congenita is a rare genetic disorder classified in clinical subtypes. Late onset of the disease has recently been described and designated as pachyonychia congenita tarda. A patient in whom typical manifestations of pachyonychia congenita appeared at the age of 39 years is described. Th...

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Published inJournal of the American Academy of Dermatology Vol. 35; no. 2; pp. 334 - 335
Main Authors Mouaci-Midoun, N, Cambiaghi, S, Abimelec, P
Format Journal Article
LanguageEnglish
Published New York, NY Mosby, Inc 01.08.1996
Elsevier
Subjects
Adult
Biological and medical sciences
Dermatology
Female
Hair and nails disorders
Humans
Medical sciences
Nail Diseases - congenital
Nail Diseases - pathology
Nails, Malformed - congenital
Nails, Malformed - pathology
Human
Case study
Skin disease
Late
Adult
Nail disease
Congenital disease
Genetic disease
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Abstract Pachyonychia congenita is a rare genetic disorder classified in clinical subtypes. Late onset of the disease has recently been described and designated as pachyonychia congenita tarda. A patient in whom typical manifestations of pachyonychia congenita appeared at the age of 39 years is described. This report substantiates previous observations on the phenomenon of late-onset pachyonychia congenita.
AbstractList Pachyonychia congenita is a rare genetic disorder classified in clinical subtypes. Late onset of the disease has recently been described and designated as pachyonychia congenita tarda. A patient in whom typical manifestations of pachyonychia congenita appeared at the age of 39 years is described. This report substantiates previous observations on the phenomenon of late-onset pachyonychia congenita.
Author Cambiaghi, S
Abimelec, P
Mouaci-Midoun, N
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Cites_doi 10.1001/archderm.1991.01680010125022
10.1016/S0190-9622(09)80144-8
10.1111/j.1365-2230.1993.tb02257.x
10.1001/archderm.1991.01680040109013
10.1111/j.1525-1470.1990.tb01070.x
10.1016/S0190-9622(88)70226-1
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Issue 2
Keywords Human
Case study
Skin disease
Late
Adult
Nail disease
Congenital disease
Genetic disease
Language English
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References Oriba, Lo, Bergfeld (BIB3) 1991; 127
Paller, Moore, Scher (BIB5) 1991; 127
Feinstein, Friedman, Schewach-Millet (BIB1) 1988; 19
Chang, Lucker, van de Kerkhof (BIB4) 1994; 30
Iraci, Bianchi, Gatti (BIB6) 1993; 18
Su, Chun, Hammond (BIB2) 1990; 7
Su (10.1016/S0190-9622(96)90663-5_BIB2) 1990; 7
Paller (10.1016/S0190-9622(96)90663-5_BIB5) 1991; 127
Feinstein (10.1016/S0190-9622(96)90663-5_BIB1) 1988; 19
Chang (10.1016/S0190-9622(96)90663-5_BIB4) 1994; 30
Oriba (10.1016/S0190-9622(96)90663-5_BIB3) 1991; 127
Iraci (10.1016/S0190-9622(96)90663-5_BIB6) 1993; 18
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  start-page: 478
  year: 1993
  end-page: 480
  ident: BIB6
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  ident: BIB5
  article-title: Pachyonychia congenita tarda
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  contributor:
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  ident: BIB2
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  ident: BIB3
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  publication-title: Pachyonychia congenita
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  ident: 10.1016/S0190-9622(96)90663-5_BIB4
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Snippet Pachyonychia congenita is a rare genetic disorder classified in clinical subtypes. Late onset of the disease has recently been described and designated as...
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SubjectTerms Adult
Biological and medical sciences
Dermatology
Female
Hair and nails disorders
Humans
Medical sciences
Nail Diseases - congenital
Nail Diseases - pathology
Nails, Malformed - congenital
Nails, Malformed - pathology
Title Pachyonychia congenita tarda
URI https://dx.doi.org/10.1016/S0190-9622(96)90663-5
https://www.ncbi.nlm.nih.gov/pubmed/8698920
https://search.proquest.com/docview/78201162
Volume 35
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