Results 81 to 90 of about 12,460 (193)

Atypical Clinical Course of Griscelli Syndrome Type 2 With Primarily Neurologic Presentation and Adult‐Onset in a 46‐Year‐Old Male

open access: yesAmerican Journal of Medical Genetics Part A, Volume 200, Issue 8, Page 1850-1855, August 2026.
ABSTRACT Griscelli Syndrome Type 2 (GS2) is a rare autosomal recessive disorder caused by pathogenic mutations in the RAB27A gene. Typically, it is characterized by cutaneous hypopigmentation, immunodeficiency, with or without neurological abnormalities secondary to hemophagocytic lymphohistiocytosis (HLH). Without treatment, GS2 often results in fatal
Dzhoy Papingi   +6 more
wiley   +1 more source

Use of Simultaneous Emission of Nd:YAG and Alexandrite Lasers in BLEND Mode for Hair Removal and Permanent Hair Reduction

open access: yesLasers in Surgery and Medicine, Volume 58, Issue 6, Page 462-473, August 2026.
Abstract Objective To evaluate the safety, efficacy, and patient satisfaction of a novel laser technology that employs simultaneous emission of Alexandrite (755 nm) and Nd:YAG (1064 nm) wavelengths for permanent hair removal, as compared with standard of care treatment using a single wavelength (either Alexandrite or Nd:Yag).
Nkemjika Ugonabo   +2 more
wiley   +1 more source

A Proposed Clinical Diagnostic Framework for Short Telomere Syndrome

open access: yesClinical Genetics, Volume 110, Issue 2, Page 139-149, August 2026.
We propose a phenotype‐based diagnostic framework for short telomere syndrome that integrates age‐adjusted telomere length, phenotypic manifestations, and genetic findings, where available. The framework is intended to guide clinical evaluation, longitudinal surveillance, and individualized management while acknowledging limitations in current telomere
Andrew Courtwright   +8 more
wiley   +1 more source

Albinism in a raccoon Procyon lotor from Mexico

open access: yesMammalogy Notes, 2021
Albinism is defined as the complete absence of pigment in skin, hair, and eyes directly caused by a hereditary disorder in the production of melanin. This genetic abnormality is usually attributed to environmental factors such as low quality of habitat ...
Rafael Flores-Peredo   +2 more
doaj  

Q‐Switched 1064‐nm Laser Versus Picosecond 1064‐nm Laser in Tattoo Removal: Comparable Overall Effectiveness With Higher Excellent Clearance Rates and Fewer Treatment Sessions for the Picosecond Laser

open access: yesJournal of Cosmetic Dermatology, Volume 25, Issue 8, August 2026.
ABSTRACT Background Laser tattoo removal is becoming more popular, with the Q‐switched (QS) 1064‐nm nanosecond laser considered the traditional standard. While the picosecond (PS) 1064‐nm laser offers an alternative for optimizing treatment protocols, comparative data regarding its relative efficacy remain limited and inconsistent.
Jiaoquan Chen   +5 more
wiley   +1 more source

5,7-Dihydroxy-4-Methylcoumarin as a Functional Compound for Skin Pigmentation and Human Skin Safety

open access: yesPharmaceuticals
Background/Objectives: This study aims to investigate the effects of 5,7-dihydroxy-4-methylcoumarin (5,7D-4MC) on melanogenesis in B16F10 murine melanoma cells and to evaluate its safety as a potential ingredient for functional cosmetics and therapeutic ...
Ye-Jin Lee, Yang Xu, Chang-Gu Hyun
doaj   +1 more source

Possible role of psoralen-induced phototoxicity in the development of vitiligo

open access: yesJAAD Case Reports, 2022
Genevieve Patrick, BS   +4 more
doaj   +1 more source

Sectoral Choroidal Hypopigmentation [PDF]

open access: yesOphthalmology, 2019
Turner D, Wibbelsman   +2 more
openaire   +2 more sources

Streaky hypopigmentation

open access: yesDermatology Online Journal, 2006
Zawar, Vijay, MD, Gugle, Anil, MD
openaire   +4 more sources

Vitiligo following COVID-19: A case report and review of pathophysiology

open access: yesJAAD Case Reports, 2022
Alexandra F. Schmidt, BS   +3 more
doaj   +1 more source

Home - About - Disclaimer - Privacy