Jadassohn Lewandowsky syndrome: Type 1 pachyonychia congenita
Pachyonychia congenita (PC) is a rare, usually autosomal dominant, genodermatosis characterized by tetrad of wedge shaped nail hypertrophy, focal palmoplantar keratoderma, oral leucokeratosis and follicular hyperkeratosis due to mutation in either of the three keratin genes, KRT6, KRT16 and KRT17. C...
Main Authors: | Anup Kumar Tiwary, Dharmendra Kumar Mishra |
---|---|
Format: | Article |
Language: | English |
Published: |
Our Dermatology Online
2017-01-01
|
Series: | Nasza Dermatologia Online |
Subjects: | |
Online Access: | http://www.odermatol.com/issue-in-html/2017-1-15-jadassohn/ |
Similar Items
-
Pachyonychia Congenita type 1 – A peerless entity
by: Yugandar Inakanti, et al.
Published: (2015-07-01) -
A Case with Pachyonychia Congenita and B-cell Lymphoma
by: Vitorino Modesto dos Santos, et al.
Published: (2014-07-01) -
Pachyonychia congenita with late onset (PC tarda)
by: A Sravanthi, et al.
Published: (2016-01-01) -
A case of type 1 pachyonychia congenita with response to acitretin
by: Bhagyashree Babanrao Supekar, et al.
Published: (2017-01-01) -
Pachyonychia congenita tarda: A rare case report
by: Ganapathi Moger, et al.
Published: (2013-01-01)