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Pachyonychia congenita (often
abbreviated as "PC") is a rare
group of
autosomal dominant skin
disorders that are
caused by a
mutation in one of five different...
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Focal palmoplantar keratoderma Papillon–Lefèvre
syndrome Pachyonychia congenita type I
Pachyonychia congenita type II
Focal palmoplantar keratoderma with...
- this
protein lead to PC-K17 (previously
known as Jackson-Lawler) type
pachyonychia congenita and
steatocystoma multiplex.
Keratin 17 has been
shown to interact...
- this
protein are ****ociated with the
genetic skin
disorders including pachyonychia congenita, non-epidermolytic
palmoplantar keratoderma and unilateral...
-
genes expressing this
protein is ****ociated with the PC-K6A
subtype of
pachyonychia congenita, an
inherited disorder of the
epithelial tissues in
which keratin...
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kindler syndrome.
Almost 1 in 50,000
people has
epidermolysis bullosa.
Pachyonychia congenita is a rare type of genodermatosis, its
clinical manifestations...
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atypical growth patterns,
including spoon-like (koilonychia) or
thickened (
pachyonychia) appearances. Skin in
individuals with ED is
frequently dry, thin, and...
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presents with
other nail
conditions such as onycholysis, koilonychia,
pachyonychia, Muehrcke's lines, leuconychia, and half-and-half nails.
Cosmetic surgery...
- Rugg EL, et al. (1997). "Missense
mutations in
keratin 17
cause either pachyonychia congenita type 2 or a
phenotype resembling steatocystoma multiplex"....
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dominant keratoderma that
represents a
clinical overlap syndrome with
pachyonychia congenita type I but
without the
classic nail involvement.: 510 Punctate...
