Laugier–Hunziker syndrome in endocrine clinical practice

Laugier–Hunziker syndrome (LHS) is a rare, benign and acquired disorder characterized by hyperpigmentation of the oral cavity and lips along with longitudinal melanonychia. No underlying systemic abnormalities or malignant predisposition is associated with it. In everyday clinical practice, an endoc...

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Detalles Bibliográficos
Autores principales: Miličević, Tanja, Žaja, Ivan, Tešanović, Deša, Radman, Maja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2018
Materias:
Unique/Unexpected Symptoms or Presentations of a Disease
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6063988/
https://www.ncbi.nlm.nih.gov/pubmed/30087778
http://dx.doi.org/10.1530/EDM-18-0025

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6063988/
https://www.ncbi.nlm.nih.gov/pubmed/30087778
http://dx.doi.org/10.1530/EDM-18-0025

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