Psoriasis
Psoriasis is a long-lasting autoimmune disease characterized by patches of abnormal skin. These skin patches are typically red, dry, itchy, and scaly. On people with darker skin the patches may be purple in colour. Psoriasis varies in severity from small, localized patches to complete body coverage. Injury to the skin[…][en.wikipedia.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]
The differential diagnosis includes inflammatory disorders such as psoriasis and lichen planus; genetic disorders such as pachyonychia congenita; as well as nail unit neoplasms[dermatologyadvisor.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]
Before the genetic basis of Pachyonychia congenita was identified and described, the disease was historically divided into the following sub-types: [8] : 510 Pachyonychia[en.wikipedia.org]
Pachyonychia congenita is a rare genetic disorder classified in clinical subtypes.[ncbi.nlm.nih.gov]
Jadassohn-Lewandowsky Syndrome
1; Pachyonychia Congenita, Jadassohn-Lewandowsky Type; Type 1 Pachyonychia Congenita; Type 2 Pachyonychia Congenita; Congenita, Pachyonychia; Jackson Lawler Type Pachyonychia[curehunter.com]
Pachyonychia congenita. J Am Acad Dermatol 1988;19:705-11. 2. Paller AS, Moore JA, Scher R. Pachyonychia congenita tarda. A late-onset form of pachyonychia congenita.[ijpd.in]
Oral Diseases (2010) 16, 310–311 Keywords: oral; eponyms; Jadassohn-Lewandowsky syndrome; Pachyonychia congenita Also known as Pachyonychia congenita The condition Jadassohn[documentslide.com]
Sebocystomatosis
In the Jackson-Lawler form (PC-2), pachyonychia is accompanied by multiple pilosebaceous cysts, natal teeth, and hair abnormalities.[ncbi.nlm.nih.gov]
Department of Medical Genetics Indiana University School of Medicine 1100 West Michigan Street Indianapolis, Indiana 46202 U.S.A Abstract Pachyonychia congenita and steatocystoma[onlinelibrary.wiley.com]
Like steatocystoma multiplex, pachyonychia congenita involves the growth of steatocystomas.[ghr.nlm.nih.gov]
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]
Chronic Arsenic Poisoning
Abstract Since 1990, a large number of people have been experiencing various health problems from drinking arsenic contaminated water (50-1860 microg/L) in 13 counties of Inner Mongolia, China, most of which are located in the Hetao Plain area. It is calculated that 411,243 people are currently at risk from arsenic[…][ncbi.nlm.nih.gov]
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.[jdr.sagepub.com]
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 ).[jdr.sagepub.com]
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]
Milium
., Bazex-Dupré-Christol syndrome, Brooke–Spiegler syndrome, oral-facial-digital syndrome type I, pachyonychia congenita.[symptoma.com]
Juvenile milia are typically found in association with assorted genetic disorders which present at birth, such as Rombo syndrome, basal cell nevus syndrome, pachyonychia congenita[ozarkderm.com]
Juvenile milia Associated with Rombo syndrome, basal cell naevus syndrome, Bazex-Dupre-Christol syndrome, pachyonychia congenita, Gardner syndrome and other genetic disorders[dermnetnz.org]