Results 131 to 140 of about 41,467 (301)

A Rare Cause of Massive Scrotal Elephantiasis: Case Report and Literature Review

Trends in Urology &Men's Health, Volume 16, Issue 6, December 2025.
ABSTRACT Scrotal lymphedema is a rare late complication of testicular cancer treatment, with most reported cases occurring in the early postoperative period. Massive scrotal elephantiasis manifesting more than a decade after postchemotherapy retroperitoneal lymph node dissection (pc‐RPLND) has not previously been described.
David Toro Tole, Jonathon Bowden, Bilal Mir, Joe Hedger, Sheshang Kamath   +4 more
wiley   +1 more source

Genotype–Phenotype Correlations, Mortality, and Clinical Insights in Keratitis–Ichthyosis–Deafness Syndrome: A Comprehensive Review and Case Report

American Journal of Medical Genetics Part A, Volume 197, Issue 11, November 2025.
ABSTRACT Keratosis–ichthyosis–deafness (KID) syndrome is a rare autosomal dominant ectodermal disease caused by mutations in the GJB2 gene, which encodes the gap junction protein Connexin 26 (Cx26) located on Chr. 13q12.11. This study presents the first mortality analysis associated with KID syndrome, focusing on a case report of a Latin American ...
Leslie Patrón‐Romero, Marco Antonio Hernández Lepe, José de Jesús Manríquez Torres, Diego Daniel Aguirre‐Gómez, Natsuo Hayashi‐Mercado, Genaro Rodríguez Uribe, Tadeo Cerón, María Ruiz‐Gamboa, Jesús Alonso Gándara‐Mireles, Ismael Lares‐Asseff, Verónica Loera‐Castañeda, Jorge Alvelais‐Palacios, Lucrecia Arzamendi‐Cepeda, Lidia Magdalena Castañeda‐González, Adolfo García‐Barrón, Francisco Yamal Quiroz Herrera, Francisco González‐Salazar, Horacio Almanza‐Reyes   +17 more
wiley   +1 more source

Colchine in dermatology [PDF]

Vojnosanitetski Pregled, 2003
Karadaglić Đorđije, Popović Milica
doaj   +1 more source

Cicatricial Alopecia of the Scalp with Keratosis Pilaris

, 1935
Louis Forman
openalex   +1 more source

A Rare Familial Case of Harlequin Ichthyosis in an Infant of a Diabetic Mother: A Diagnostic and Management Challenge in Low and Middle Income Settings

Clinical Case Reports, Volume 13, Issue 11, November 2025.
ABSTRACT Harlequin Ichthyosis (HI) is an extremely rare, autosomal recessive, and highly fatal condition in neonates. It is especially difficult to control in the low‐ and middle‐income countries (LMICs) due to the low rate of prenatal screening, cultural reluctance, and lack of access to neonatal intensive care.
Muhammad Zaeem, Ameer Hamza Mehmood Ul Hassan, Muhammad Hassaan Javaid, Muhammad Usman, Muhammad Ahmed, Muhammad Usama Naveed, Mohammad Yassin Al Aboud   +6 more
wiley   +1 more source

Effect of a Low-Fat Diet on the Incidence of Actinic Keratosis [PDF]

, 1994
Homer S. Black, J. Alan Herd, Leonard H. Goldberg, John E. Wolf, John I. Thornby, Theodore Rosen, Suzanne Bruce, Jaime A. Tschen, John P. Foreyt, Lynne W. Scott, Suzanne Jaax, Kelly Andrews   +11 more
openalex   +1 more source

Simulated daylight vs. conventional PDT for clinical superficial BCC: A randomized controlled trial

Journal of the European Academy of Dermatology and Venereology, Volume 39, Issue 11, Page 1997-2004, November 2025.
In this single‐centre, non‐inferiority, randomized controlled trial, SDL‐PDT (n = 95 lesions) was less effective than C‐PDT (n = 98 lesions) in treating superficial basal cell carcinoma One‐year clearance rates: 61.3% with SDL‐PDT versus 91.8% with C‐PDT (p < 0.001).
Alexandra Sjöholm, Eva Backman, Maja Modin, Julia Fougelberg, Magdalena Claeson, John Paoli   +5 more
wiley   +1 more source

Genetic linkage evaluation of twenty-four loci in an eastern Canadian family segregating Darier's disease (keratosis follicularis) [PDF]

, 1994
Deborah Sidenberg, Daniel Berg, A.S. Bassett, Nicole King, Artūras Petronis, Arvind Baburao Kamble, James Kennedy   +6 more
openalex   +1 more source

KT‐939: A Next‐Generation Human Tyrosinase Inhibitor With Superior Efficacy for the Safe Management of Hyperpigmentation

Journal of Cosmetic Dermatology, Volume 24, Issue 11, November 2025.
ABSTRACT Background Tyrosinase is the rate‐limiting enzyme in melanin biosynthesis, and its overactivity contributes to hyperpigmentation disorders. Existing tyrosinase inhibitors are often limited by poor potency against human tyrosinase (hTYR) or safety concerns. Aims To evaluate the inhibitory potency, safety, and multifunctional activity of KT‐939,
Xiaodan Hou, Yunhui Li, Qun Zhang, Honghua Yan, Xin Zhang, Yueying Yang, Xiang Cai, Jin Wang, Miaohua Ding, Dong Chen, Jie Chen, Youzhi Tong, Nina Mehta, Andy Goren   +13 more
wiley   +1 more source

Addressing the Diagnostic Odyssey for Adults With Neurodevelopmental Disabilities: Case Study of an Individual With Mandibulofacial Dysostosis With Microcephaly

American Journal of Medical Genetics Part A, Volume 197, Issue 10, October 2025.
ABSTRACT Whole exome sequencing (WES) has been widely used in the pediatric setting to increase diagnostic yield, provide treatment options, and to estimate reoccurrence risks. However, there is limited knowledge regarding the utility of this technology in adults with neurodevelopmental disabilities.
Ruhi Shah, Neora Shifrin, Mary Ellen Keogh, Elaine Marchi, Maureen Gavin, Karen Amble, Gholson J. Lyon   +6 more
wiley   +1 more source