Pachyonychia congenita: A rare genodermatosis

Pachyonychia congenita (PC) is a rare genodermatosis with only 450 cases reported since 1906. It is of two types, type I due to mutation in genes 6a and 16, and 6b and 17 in type II with an autosomal dominant inheritance in both types. A 22 yr old female patient presented in our OPD with hypertrophy...

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Detaylı Bibliyografya
Asıl Yazarlar: Agarwal, Puneet, Chhaperwal, Mahendra K., Singh, Apurva, Verma, Arvind, Nijhawan, Manisha, Singh, Kishore, Mathur, Dinesh
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Medknow Publications & Media Pvt Ltd 2013
Konular:
Case Report
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3752484/
https://ncbi.nlm.nih.gov/pubmed/23984242
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/2229-5178.115527
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