Possible Causes for pachyonychia Ovarian Cyst Pachyonychia congenita cornered: report on the 11th Annual International Pachyonychia Congenita Consortium Meeting. [ghr.nlm.nih.gov] Oral lesions accompanying pachyonychia congenital. Oral Surg 1958;11:541-4. [PUBMED] 16. Hannaford RS, Stapleton K. Pachyonychia congenita tarda. [jiaomr.in] How is pachyonychia congenita diagnosed? Pachyonychia congenita is usually diagnosed by its clinical appearance. [dermnetnz.org] Psoriasis Back to Journals » Drug Design, Development and Therapy » Volume 7 Review Authors Palfreeman A, McNamee KE, McCann FE Received 1 December 2012 Accepted for publication 19 January 2013 Published 27 March 2013 Volume 2013:7 Pages 201—210 DOI Checked for plagiarism Yes Review by Single-blind Peer reviewer comments 4[…] [doi.org] Upper Urinary Tract Infection Pachyonychia congenita cornered: report on the 11th Annual International Pachyonychia Congenita Consortium Meeting. [ghr.nlm.nih.gov] Svenska synonymer Jadassohn-Lewandowskys syndrom Engelska synonymer Pachyonychia Congenita Syndrome — Congenital Pachyonychia — Pachyonychia, Congenital — Pachyonychia Congenita [mesh.kib.ki.se] How is pachyonychia congenita diagnosed? Pachyonychia congenita is usually diagnosed by its clinical appearance. [dermnetnz.org] Onychomycosis There was no family history of psoriasis, Darier's disease, pachyonychia congenita, or lichen planus. [jamanetwork.com] Pachyonychia congenita This is a rare condition but must be excluded in children with thick nails. [tandfonline.com] Pachyonychia congenita – Marked subungual hyperkeratosis with accumulation of hard keratinous material resulting in uplifting of the nail plate. [visualdx.com] Pachyonychia Congenita Congenita Jadassohn-Lewandowsky Syndrome PACHYONYCHIA CONGENITA, JADASSOHN-LEWANDOWSKY TYPE Pachyonychia Congenita Type 1 edit English pachyonychia congenita rare group of [wikidata.org] Pachyonychia congenita Pachyonychia congenita has an autosomal dominant pattern of inheritance. [en.wikipedia.org] Pachyonychia congenita is a rare genetic disorder classified in clinical subtypes. [ncbi.nlm.nih.gov] Pancytopenia Pachyonychia congenita cornered: report on the 11th Annual International Pachyonychia Congenita Consortium Meeting. [ghr.nlm.nih.gov] Oral lesions accompanying pachyonychia congenital. Oral Surg 1958;11:541-4. [PUBMED] 16. Hannaford RS, Stapleton K. Pachyonychia congenita tarda. [jiaomr.in] How is pachyonychia congenita diagnosed? Pachyonychia congenita is usually diagnosed by its clinical appearance. [dermnetnz.org] Diffuse Palmoplantar Keratoderma Pachyonychia congenita is a very close differential diagnosis for this entity. [ncbi.nlm.nih.gov] Pachyonychia congenita 5. Focal PPK associated w/esophageal carcinoma 32. [slideshare.net] It is seen commonly in pachyonychia congenita with prominent nail involvement. [ijpd.in] Pachyonychia Congenita Type 1 Congenita Jadassohn-Lewandowsky Syndrome PACHYONYCHIA CONGENITA, JADASSOHN-LEWANDOWSKY TYPE Pachyonychia Congenita Type 1 edit English pachyonychia congenita rare group of [wikidata.org] Rittié, Pachyonychia congenita cornered: report on the 11th Annual International Pachyonychia Congenita Consortium Meeting, British Journal of Dermatology, 171, 5, (974-977 [doi.org] PACHYONYCHIA CONGENITA, JADASSOHN-LEWANDOWSKY TYPE Pachyonychia Congenita Type 1 Statements Identifiers Sitelinks Wikipedia (8 entries) edit Wikibooks (0 entries) edit Wikiquote [wikidata.org] Palmoplantar Keratosis Pachyonychia congenita Orphanet Encylopedia., ( online PDF ) accessed 21/12/2008. 5. Thost A. Über erbliche Ichtyosis palmaris et plantaris cornea. Dissertation. [faoj.org] Costa (10) Arsenhyperkeratosen (4) Dyskeratosis congenita (12) Fokale akrale Hyperkeratose (12) Hyperkeratotisch-rhagadiformes Hand- / Fußekzem (8) Lichen ruber planus (102) Pachyonychia [dermis.net] Congenita KRT17-Related Pachyonychia Congenita KRT6A-Related Pachyonychia Congenita KRT6B-Related Pachyonychia Congenita Keratitis-Ichthyosis-Deafness Syndrome, Autosomal [genetests.org] Laryngeal Obstruction A 2-year-old girl presented with typical clinical features of pachyonychia congenita shortly after birth. [ncbi.nlm.nih.gov] Pachyonychia congenita is a genetic syndrome of epithelial dysplasia. [ncbi.nlm.nih.gov] Pachyonychia congenita is a rare genodermatosis that can affect the larynx. Laryngeal obstruction is very unusual with only a few cases reported. [ncbi.nlm.nih.gov] Sebocystomatosis In the Jackson-Lawler form (PC-2), pachyonychia is accompanied by multiple pilosebaceous cysts, natal teeth, and hair abnormalities. [ncbi.nlm.nih.gov] Like steatocystoma multiplex, pachyonychia congenita involves the growth of steatocystomas. [ghr.nlm.nih.gov] In the familial form of steatocystoma multiplex, mutations are localized to the keratin 17 ( K17 ) gene in areas identical to mutations found in patients with pachyonychia [emedicine.medscape.com] Steatocystoma Multiplex With Natal Teeth “Pachyonychia congenita”. 1996. pp. 246-7. (A clinical guide to identifying, diagnosing, and treating pachyonychia congenita.) Haber, RM. “Drummond D. [dermatologyadvisor.com] Keywords: Late onset pachyonychia congenita, pachyonychia congenita, Pachyonychia congenita tarda How to cite this article: Sravanthi A, Srivalli P, Gopal K, Rao T N. [idoj.in] A study in pachyonychia congenita. Clin Exp Dermatol. 2016; 41:26-33. [rarediseases.org] White Sponge Nevus Leukoedema may be confused with leukoplakia, Darier's disease, white sponge nevus, pachyonychia congenita, or candidal infection. [ncbi.nlm.nih.gov] Keratin 16 and keratin 17 mutations cause pachyonychia congenita. Nat Genet 9: 273 - 278. [doi.org] Mutation of a type II keratin gene (K6a) in pachyonychia congenita. Nat Genet 10:363365. Google Scholar Crossref Medline ISI Browne WG, Izatt MM, Renwick JH ( 1969 ). [doi.org] Hidrotic Ectodermal Dysplasia Clouston syndrome can mimic pachyonychia congenita. J Invest Dermatol. 2003 Nov;121(5):1035-8 Lamartine et al. Mutations in GJB6 cause hidrotic ectodermal dysplasia. [genedx.com] Clouston syndrome can mimic pachyonychia congenita. [ncbi.nlm.nih.gov] Pachyonychia congenita is caused by a pathogenic variant in one of the following genes: KRT6A, KRT6B, KRT6C, KRT16, or KRT17. [ncbi.nlm.nih.gov] Chronic Arsenic Poisoning Microvasc Res. 2008 Nov;76(3):194-201. doi: 10.1016/j.mvr.2008.07.001. Epub 2008 Jul 11. Author information 1 Department of Dermatology, Kaohsiung Medical University Hospital and College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan. Abstract An endemic peripheral vascular disorder due to chronic arsenic[…] [ncbi.nlm.nih.gov] Milium Juvenile milia Associated with Rombo syndrome, basal cell naevus syndrome, Bazex-Dupre-Christol syndrome, pachyonychia congenita, Gardner syndrome and other genetic disorders [dermnetnz.org] Associated with Rombo syndrome, basal cell naevus syndrome, Bazex-Dupre-Christol syndrome, pachyonychia congenita, Gardner syndrome and other genetic disorders 2. [dermnetnz.org] Congenital Leukonychia […] disorder 5 nonsyndromic congenital nail disorder 6 nonsyndromic congenital nail disorder 7 nonsyndromic congenital nail disorder 8 Odontomicronychial Dysplasia Onycholysis pachyonychia [rgd.mcw.edu] Congenital malformation of hair NOS Persistent lanugo Q84.3 Anonychia Q84.4 Congenital leukonychia Q84.5 Enlarged and hypertrophic nails Inclusion term(s): Congenital onychauxis Pachyonychia [icd10coded.com] […] congenita syndrome Pachyonychia congenita type II of Jackson-Lawler Pachyonychia congenita type III of Schafer-Brunauer Polyonychia Racket nail Ridged nails Splinter hemorrhages [icd9data.com] Exostosis Part II: acquired localized longitudinal pachyonychia and masked nail tumors. Am J Dermatopathol 2013;35:693-709. [karger.com] On examination, oyster shell nail plates were found, and, therefore, pachyonychia (the noncongenital type) was suspected. [karger.com] Congenital Onychodysplasia […] congenita syndrome Pachyonychia congenita type II of Jackson-Lawler Pachyonychia congenita type III of Schafer-Brunauer Polyonychia Racket nail Ridged nails Splinter hemorrhages [icd9data.com] In 1991, Paller et al., have reported a late-onset form, termed 'pachyonychia congenita tarda'. In these cases pachyonychia is apparent during the teenage years. [handresearch.com] Congenita 1 Pachyonychia Congenita 2 Palmoplantar Keratoderma and Congenital Alopecia 2 Palmoplantar Keratoderma and Congenital Alopecia, Autosomal Dominant Papillon-Lefevre [nfed.org] Howell-Evans Syndrome ‘woolly’ hair from birth Focal keratoderma develops in infancy Heart disease develops in adolescence May result in clubbing of the nails Blistering of the skin may occur Pachyonychia [dermnetnz.org] Pachyonychia congenita 5. Focal PPK associated w/esophageal carcinoma 32. [de.slideshare.net] […] children have mental retardation Restriction of phenylalanine and tyrosine in the diet is required to improve symptoms and may prevent the progression of mental retardation Pachyonychia [dermnetnz.org] Ectodermal Dysplasia The phenotypic and molecular genetic features of pachyonychia congenita. J Invest Dermatol. 2011 May. 131 (5):1015-7. [Medline]. [emedicine.com] […] differential considerations include: alopecia areata aplasia cutis congenita focal dermal hypoplasia syndrome incontinentia pigmenti Naegeli-Franceschetti-Jadassohn syndrome pachyonychia [radiopaedia.org] Pachyonychia congenita in pediatric patients: natural history, features, and impact. JAMA Dermatol. 2014 Feb. 150 (2):146-53. [Medline]. [emedicine.com] Pfeiffer-Palm-Teller Syndrome Pachydermoperiostosis Pachygyria Pachygyria with mental retardation and seizures Pachygyria frontotemporal Pachyonychia congenita Pachyonychia congenita type 1 Pachyonychia [personalizedcause.com] Congenita 1; PC1 OMIM:167210 Pachyonychia Congenita 2; PC2 OMIM:615726 Pachyonychia Congenita 3; PC3 OMIM:615728 Pachyonychia Congenita 4; PC4 OMIM:260130 Pachyonychia Congenita [informatics.jax.org] A B C D E F G H I J K L M N O P Q R S T U V W X Y Z Pa-Pd Pachydermoperiostosis Pachygyria Pachyonychia congenita Jackson Lawler type Pacman syndrome Paes Whelan Modi syndrome [bioreference.net] Ganglion Cyst Steatocystoma multiplex is sometimes an autosomal dominantly inherited disorder due to mutations localised to the keratin 17 (K17) gene, when it may be associated with pachyonychia [dermnetnz.org] Acne Vulgaris […] although its efficacy is increased in combination with PUVA therapy, and in rare conditions such as x-linked ichthyosis, bullous congenital ichthyosiform erythroderma and pachyonychia [doi.org] Spondyloepimetaphyseal Dysplasia-Hypotrichosis Syndrome […] congenita 1 (PC1) [MIM: 167200 ] KRT6B P04259 non-pleiotropic Pachyonychia congenita 2 (PC2) [MIM: 167210 ] KRT74 Q7RTS7 pleiotropic Woolly hair autosomal dominant (ADWH) [sbg.bio.ic.ac.uk] […] congenita type 1 KRT16 Pachyonychia congenita type 2 KRT17 Pachyonychia congenita type 3 KRT6A Pachyonychia congenita type 4 KRT6B Paget disease of bone SQSTM1 Paget disease [centogene.com] […] congenita type 1 (KRT16) Cost: 30000.00 Test Offer Pachyonychia congenita type 2 (KRT17) Cost: 30000.00 Test Offer Pachyonychia congenita type 3 (KRT6A) Cost: 30000.00 Test [dnalabsindia.com] Epidermolysis Bullosa Simplex BACKGROUND: Painful foot blistering is a common problem in patients with epidermolysis bullosa simplex (EBS) and pachyonychia congenita (PC). [ncbi.nlm.nih.gov] On physical examination as an adult, we observed diffuse non-scarring alopecia on the scalp, onychodystrophy (pachyonychia) in all 20 nails, dental decay, mild dysphonia, [ncbi.nlm.nih.gov] Smith, Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita, Journal of Investigative Dermatology, 132, 7, (1921 [dx.doi.org] Congenital Ankyloblepharon “Pachyonychia congenita”. 1996. pp. 246-7. (A clinical guide to identifying, diagnosing, and treating pachyonychia congenita.) Haber, RM. “Drummond D. [dermatologyadvisor.com] Congenita 1 Pachyonychia Congenita 2 Palmoplantar Keratoderma and Congenital Alopecia 2 Palmoplantar Keratoderma and Congenital Alopecia, Autosomal Dominant Papillon-Lefevre [nfed.org] Enrollment in the International Pachyonychia Congenita Research Registry and involvement with the Pachyonychia Congenita Project should be offered for social support and patient [dermatologyadvisor.com] Prata-Libéral-Gonçalves Syndrome PEPCK deficiency, mitochondrial Pachyonychia congenita Jackson Lawler type Paes Whelan Modi syndrome Paget disease extramammary Paget disease juvenile type Paget's disease [mindmappedia.com] A B C D E F G H I J K L M N O P Q R S T U V W X Y Z Pa-Pd Pachydermoperiostosis Pachygyria Pachyonychia congenita Jackson Lawler type Pacman syndrome Paes Whelan Modi syndrome [bioreference.net] Pachyonychia congenita Jackson Lawler type[?] Pacman syndrome[?] Paes Whelan Modi syndrome[?] Paget disease extramammary[?] Paget disease juvenile type[?] [encyclopedia.kids.net.au] Atopic Dermatitis the Pachyonychia Congenita Project (F.J.D.S.), the British Skin Foundation/National Eczema Society (F.J.D.S. & W.H.I.M.), the Biotechnology and Biological Sciences Research [doi.org] Patterson Pseudoleprechaunism Syndrome Pachydermoperiostosis Pachygyria Pachygyria with mental retardation and seizures Pachygyria frontotemporal Pachyonychia congenita Pachyonychia congenita type 1 Pachyonychia [personalizedcause.com] Congenita 1; PC1 OMIM:167210 Pachyonychia Congenita 2; PC2 OMIM:615726 Pachyonychia Congenita 3; PC3 OMIM:615728 Pachyonychia Congenita 4; PC4 OMIM:260130 Pachyonychia Congenita [informatics.jax.org] OMIM:600356 Pachydermodactyly, Familial OMIM:610279 Pachygyria, Frontotemporal OMIM:600176 Pachygyria with Mental Retardation, Seizures, and Arachnoid Cysts OMIM:167200 Pachyonychia [informatics.jax.org]
