Results 11 to 20 of about 16,794 (254)

A Prospective Interventional Study of Xanthelasma Palpebrarum Treated with Ultrapulse Carbon Dioxide Laser [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2021
Introduction: Xanthelasma palpebrarum (XP) is the most common of all the xanthomas which presents as asymptomatic, often bilateral, soft, yellow, papules and plaques around the eyelids. Although, the lesions are benign, it is aesthetically upsetting.
Manjeet Naresh RamtekE   +1 more
doaj   +1 more source

A gain-of-function TPC2 variant R210C increases affinity to PI(3,5)P2 and causes lysosome acidification and hypopigmentation

open access: yesNature Communications, 2023
Albinism is a group of inherited disorders mainly affecting skin, hair and eyes. Here we identify a de novo point mutation, p.R210C, in the TPCN2 gene which encodes Two Pore Channel 2 (TPC2) from a patient with albinism.
Qiaochu Wang   +14 more
semanticscholar   +1 more source

Post-Inflammatory Hypopigmentation: Review of the Etiology, Clinical Manifestations, and Treatment Options

open access: yesJournal of Clinical Medicine, 2023
Post-inflammatory hypopigmentation is a common acquired pigmentary disorder that is more prominent in skin of color, leading to great cosmetic and psychosocial implications.
M. Rao   +4 more
semanticscholar   +1 more source

The Hypopigmentation Mechanism of Tyrosinase Inhibitory Peptides Derived from Food Proteins: An Overview

open access: yesMolecules, 2022
Skin hyperpigmentation resulting from excessive tyrosinase expression has long been a problem for beauty lovers, which has not yet been completely solved.
Y. Song   +4 more
semanticscholar   +1 more source

A novel pathogenic RHOA variant in a patient with patterned cutaneous hypopigmentation associated with extracutaneous findings

open access: yesPediatric dermatology, 2022
RHOA‐related neuroectodermal syndrome is characterised by linear skin hypopigmentation along Blaschko's lines associated with alopecia, leukoencephalopathy, facial and limb hypoplasia, and ocular, dental, and acral anomalies.
Z. R. Cai   +4 more
semanticscholar   +1 more source

Pigmentary abnormality without significant drusen as a risk factor for late age-related macular degeneration

open access: yesScientific Reports, 2022
We investigated the incidence and risk factors of late age-related macular degeneration (AMD) in the fellow eye (FE) without significant drusen of patients with unilateral exudative macular neovascularization (MNV).
Junwon Lee   +6 more
doaj   +1 more source

Perifollicular Hypopigmentation in Systemic Sclerosis: Associations With Clinical Features and Internal Organ Involvement

open access: yesJournal of Rheumatology, 2022
Objective To determine whether perifollicular hypopigmentation in systemic sclerosis (SSc) is associated with demographics, distinct clinical features, and autoantibody profiles.
M. Chung   +4 more
semanticscholar   +1 more source

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