Abstract Peutz‑Jeghers syndrome (PJS), a rare autosomal dominant serine/threonine kinase
11 (STK11)/liver kinase B1 (LKB1) gene‑related genodermatosis, is characterized by oral …

Peutz-Jeghers syndrome (PJS) is a well-described inherited syndrome, characterized by the
development of gastrointestinal polyps and characteristic mucocutaneous freckling. PJS is …

This review highlights oral anomalies with major clinical impact in Addison disease (AD),
including dental health and dermatologic features, through a dual perspective: pigmentation …

Objectives: Identify the etiology of Laugier-Hunziker syndrome. Explain the key
differentiating features specific to Laugier-Hunziker syndrome. Assess the management …

Laugier–Hunziker syndrome: an exceptional cause of acquired hyperpigmentation Page 1 © Our
Dermatol Online e.2021 1 Our Dermatology Online Laugier–Hunziker syndrome: an exceptional …

El síndrome de Laugier-Hunziker (SLH) es un trastorno de hiperpigmentación macular
benigno adquirido que se caracteriza por la presencia de máculas hiperpigmentadas …

Laugier–Hunziker syndrome (LHS) is a rare, benign pigmentary disorder characterized by
unique pigmentation over mucosa, nails, and acral sites, arising spontaneously during …

Laugier-Hunziker syndrome (LHS) is an acquired benign macular hyperpigmentation
disorder, characterized by the presence of polychromic hyperpigmented macules, with a …

This review highlights oral anomalies with major clinical impact in Addison disease (AD),
including dental health and dermatologic features, through a dual perspective: pigmentation …

Background Melanonychia is brown or black pigmentation of the nail unit. Melanonychia
commonly presents as pigmented band arranged lengthwise along the nail unit, and this …