Literature DB >> 12894104

Familial Laugier-Hunziker syndrome.

Edouard N Makhoul1, Nakhlé M Ayoub, Josiane F Helou, Gerard A Abadjian.   

Abstract

We report the unusual occurrence of 3 cases of Laugier-Hunziker syndrome in the same family.

Entities:  

Mesh:

Year:  2003        PMID: 12894104     DOI: 10.1067/mjd.2003.300

Source DB:  PubMed          Journal:  J Am Acad Dermatol        ISSN: 0190-9622            Impact factor:   11.527


  7 in total

1.  A review of the diverse genetic disorders in the Lebanese population: highlighting the urgency for community genetic services.

Authors:  Ghunwa Nakouzi; Khalil Kreidieh; Soha Yazbek
Journal:  J Community Genet       Date:  2014-09-27

Review 2.  [Pigmented lesions of the genital mucosa].

Authors:  U R Hengge; M Meurer
Journal:  Hautarzt       Date:  2005-06       Impact factor: 0.751

3.  Laugier-hunziker syndrome: a rare cause of oral and acral pigmentation.

Authors:  Silonie Sachdeva; Shabina Sachdeva; Pranav Kapoor
Journal:  J Cutan Aesthet Surg       Date:  2011-01

4.  Laugier-Hunziker syndrome in a patient with rheumatoid arthritis.

Authors:  Ayşe Ünal Enginar; Nehir Samancı Karaman; Ayşe Akman Karakaş
Journal:  Reumatologia       Date:  2019-02-28

5.  Clinical and histopathological differential diagnosis of Laugier-Hunziker syndrome: An extremely rare case with unusual extensive oral hyperpigmentation.

Authors:  Verena Toedtling; Fiona Carol Crawford
Journal:  Clin Case Rep       Date:  2020-11-16

6.  Laugier-Hunziker syndrome.

Authors:  Ramakant S Nayak; Vijayalakshmi S Kotrashetti; Jagadish V Hosmani
Journal:  J Oral Maxillofac Pathol       Date:  2012-05

Review 7.  Mystery behind labial and oral melanotic macules: Clinical, dermoscopic and pathological aspects of Laugier-Hunziker syndrome.

Authors:  Ning Duan; Yang-Heng Zhang; Wen-Mei Wang; Xiang Wang
Journal:  World J Clin Cases       Date:  2018-09-26       Impact factor: 1.337

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.