Pachyonychia Congenita, Jadassohn Lewandowsky Type

Known as: PACHYONYCHIA CONGENITA, JADASSOHN-LEWANDOWSKY TYPE, FORMERLY, PACHYONYCHIA CONGENITA 1, JADASSOHN-LEWANDOWSKY SYNDROME, FORMERLY 
A subtype of pachyonychia congenita that is associated with mutations in the gene for KERATIN-16 and the gene for KERATIN-6A.

Topic mentions per year

Topic mentions per year

1969-2015
02419692015

Papers overview

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Review
2016
Review
2016
The case of an 8-year-old boy is hereby reported, who presented with nail dystrophy, subungual hyperkeratosis, oral… (More)
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Review
2016
2015
2015
Pachyonychia congenita (PC) is a rare autosomal dominant genodermatosis characterized by hyperkeratosis affecting the nails and… (More)
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2014
2014
Pachyonychia congenital (PC), consist of a group of rare autosomal-dominant ectodermal disorders. Symmetrically thickened… (More)
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2013
2013
Pachyonychia congenita (PC) is a rare genodermatosis with only 450 cases reported since 1906. It is of two types, type I due to… (More)
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2000
2000
Die Pachyonychia congenita (PC) ist eine seltene, meist autosomal dominat vererbbare, ektodermale Dysplasie mit variabler Ph… (More)
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2000
2000
Pachyonychia congenita type 1 (PC-1) is an autosomal dominant ectodermal dysplasia characterized by nail dystrophy, focal non… (More)
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1997
1997
Pachyonychia congenita (PC) is a group of autosomal dominant ectodermal dysplasias in which the main phenotypic characteristic is… (More)
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1995
1995
Pachyonychia congenita (PC) is a rare autosomal dominant condition characterized by multiple ectodermal abnormalities1–3… (More)
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1987
1987
Pachyonychia congenita (Jadassohn-Lewandowsky Syndrome) is a rare autosomal dominant disorder characterized by nail dystrophy… (More)
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