Cargando...
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...
Gardado en:
| Publicado en: | Endocrinol Diabetes Metab Case Rep |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Bioscientifica Ltd
2018
|
| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6063988/ https://ncbi.nlm.nih.gov/pubmed/30087778 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1530/EDM-18-0025 |
| Tags: |
Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!
|