Create a free QxMD account to receive personalized paper recommendations, relevant to your practice.

Get Started

LETTER

Haber's syndrome may be a clinical entity different from Dowling-Degos disease

A Nishizawa, H Nakano, T Satoh, K Takayama, D Sawamura, H Yokozeki

British Journal of Dermatology 2009, 160 (1): 215-7

No abstract text is available yet for this article.

Full Text Links

Find Full Text Links for this Article

You are not logged in. Sign Up or Log In to join the discussion.

Coexistent Dowling-Degos disease and reticulate acropigmentation of kitamura with progressive seborrheic keratosis. Zhu Shen, Ling Chen, Qingyi Ye, Fei Hao, Modesto dos Santos Vitorino, Xichuan Yang, Baiyu Zhong Cutis; Cutaneous Medicine for the Practitioner 2011, 87 (2): 73-5

Haber's syndrome. C J McCormack, P Cowen Australasian Journal of Dermatology 1997, 38 (2): 82-4

Systematic mutation screening of KRT5 supports the hypothesis that Galli-Galli disease is a variant of Dowling-Degos disease. S Hanneken, A Rütten, S M Pasternack, S Eigelshoven, L El Shabrawi-Caelen, J Wenzel, M Braun-Falco, T Ruzicka, M M Nöthen, R Kruse, R C Betz British Journal of Dermatology 2010, 163 (1): 197-200

Generalized Dowling-Degos disease. Yu-Hung Wu, Yang-Chih Lin Journal of the American Academy of Dermatology 2007, 57 (2): 327-34

Haber's syndrome or Dowling-Degos disease? I Kikuchi Archives of Dermatology 1983, 119 (5): 365-6

Galli-Galli disease is an acantholytic variant of Dowling-Degos disease. E Sprecher, M Indelman, Z Khamaysi, J Lugassy, D Petronius, R Bergman British Journal of Dermatology 2007, 156 (3): 572-4

Weary-Kindler syndrome with multiple seborrheic keratoses. A Y Kapasi, U Khopkar, S Raj, S L Wadhwa International Journal of Dermatology 1993, 32 (6): 444-5

Haber's syndrome or Dowling-Degos disease? F Crovato, A Rebora Archives of Dermatology 1982, 118 (4): 214

FGFR3 and PIK3CA mutations in stucco keratosis and dermatosis papulosa nigra. C Hafner, M Landthaler, T Mentzel, T Vogt British Journal of Dermatology 2010, 162 (3): 508-12

Make the most of Read.
Download the mobile app.

Use Read by QxMD to access full text via your institution or open access sources.

Read also provides personalized recommendations to keep you up to date in your field.

Existing User

New to Read

Read