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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protein lead to PC-K17 (previously known as Jackson-Lawler) type pachyonychia congenita and steatocystoma multiplex. Keratin 17 has been shown to interact...
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protein are associated with the genetic skin disorders including pachyonychia congenita, non-epidermolytic palmoplantar keratoderma and unilateral palmoplantar...
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palmoplantar keratoderma Papillon–Lefèvre syndrome Pachyonychia congenita type I Pachyonychia congenita type II Focal palmoplantar keratoderma with oral...
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Genodermatosis (section Pachyonychia congenita)
syndrome. Almost 1 in 50,000 people has epidermolysis bullosa. Pachyonychia congenita is a rare type of genodermatosis, its clinical manifestations are...
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expressing this protein is associated with the PC-K6A subtype of pachyonychia congenita, an inherited disorder of the epithelial tissues in which keratin...
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et al. (1997). "Missense mutations in keratin 17 cause either pachyonychia congenita type 2 or a phenotype resembling steatocystoma multiplex". J. Invest...
6 KB (633 words) - 07:32, 22 October 2023
syndrome/Dermatopathia pigmentosa reticulariss is associated with KRT14. Pachyonychia congenita is caused by multiple keratins. Focal dermal hypoplasia is associated...
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keratoderma syndrome, oculo-dento-digital syndrome, pachyonychia congenita-2, Rapp-Hodgkin syndrome, Reeds syndrome, Salamon syndrome, Schöpf-Schulz-Passarge...
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biomedical image processing Pubococcygeus muscle Parietal cell Pachyonychia congenita, a genetic skin disorder Pancreatic cancer Prostate cancer Palliative...
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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...
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NCT00689065 TD101 K6a (N171K mutation) Naked siRNA Pachyonychia congenita I Completed Pachyonychia Congenita Project NCT00716014 AGN211745 VEGFR1 Naked siRNA...
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Touraine) Pachyonychia congenita type I (Jadassohn–Lewandowsky syndrome) Pachyonychia congenita type II (Jackson–Lawler pachyonychia congenita, Jackson–Sertoli...
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(see: Leukoplakia with tylosis and esophageal carcinoma). Dyskeratosis congenita may be associated with leukoplakia of the oral mucosa and of the anal...
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subtype of pachyonychia congenita. McLean WH, Rugg EL, Lunny DP, et al. (March 1995). "Keratin 16 and keratin 17 mutations cause pachyonychia congenita". Nat...
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also Health Exercise Nutrition Pachydermoperiostosis Pachygyria Pachyonychia congenita Jackson–Lawler type Pacman dysplasia Paes–Whelan–Modi syndrome Paget...
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include:[citation needed] Palmoplantar ectodermal dysplasia type 1 or Pachyonychia congenita type I Palmoplantar ectodermal dysplasia type 3 or Acrokeratoelastoidosis...
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Schwartz ME, Rittié L (2014). "Pachyonychia congenita cornered: report on the 11th Annual International Pachyonychia Congenita Consortium Meeting". Br. J...
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skin disorders, including psoriasis, epidermolysis bullosa, and pachyonychia congenita. Type I keratin Schweizer, Jürgen; Bowden, Paul E.; Coulombe, Pierre...
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palmoplantar verrucous nevus is a cutaneous condition that has features of pachyonychia congenita. Unilateral nevoid telangiectasia List of cutaneous conditions Rapini...
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onychogryposis, hyperkeratosis, leukoplakia, hyperhidrosis and pachyonychia congenita. Nevus Sebaceous of Jadassohn: yellow-orange flat plaque, occurring...
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EIF2B5 Pachyonychia congenita Jackson Lawler type; 167210; KRT17 Pachyonychia congenita Jackson Lawler type; 167210; KRT6B Pachyonychia congenita, Jadassohn-Lewandowsky...
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domain Drug Indication Target Ocular and retinal disorders TD101 Pachyonychia congenita Keratin 6A N171K mutant Ocular and retinal disorders QPI-1007 Non-arteritic...
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Papillon–Lefèvre syndrome Haim–Munk syndrome Premature dentition (Natal teeth) Pachyonychia congenita type II Grey–green discoloration of the mid-portion of permanent...
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hydroxychloroquine. Pachyonychia Congenita. The Pachyonychia Congenita Quality of Life (PCQoL) was developed in 2012 to determine the effect Pachyonychia Congenita has...
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Siemens skin KRT2A Palmoplantar keratoderma skin KRT1, KRT9, KRT16 Pachyonychia congenita skin KRT6A, KRT6B, KRT16, KRT17 White sponge nevus skin KRT4, KRT13...
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simplex Dowling–Degos' disease Olmsted syndrome 6a Pachyonychia congenita type I 6b Pachyonychia congenita type II 7 8 9 Diffuse epidermolytic palmoplantar...
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Dowling–Degos' disease Olmsted syndrome KRT6A Pachyonychia congenita type I KRT6B Pachyonychia congenita type II KRT9 Diffuse epidermolytic palmoplantar...
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gingival keratosis Howel–Evans syndrome Pachyonychia congenita Pachyonychia congenita type I Pachyonychia congenita type II Striate palmoplantar keratoderma...
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epidermis, its appendages and other epithelial tissues, including pachyonychia congenita, muscular dystrophy with epidermolysis bullosa simplex and Meesmann...
14 KB (1,060 words) - 12:24, 7 October 2024