Results 221 to 230 of about 50,269 (341)

A 17‐Year‐Old Girl With an Unusual Inflamed Papule on the Forearm

Pediatric Dermatology, EarlyView.
Zara Nadir, Tiffaney Tran, Susuana Adjei, Stephen K. Tyring   +3 more
wiley   +1 more source

An Ocular Manifestation of a Systemic Disease With Encephalitozoon Pogonae in a Juvenile Central Bearded Dragon (Pogona vitticeps)

Veterinary Ophthalmology, EarlyView.
ABSTRACT Objective Encephalitozoon pogonae, a recently identified microsporidian species, has been associated with systemic infections in Central bearded dragons (Pogona vitticeps) manifesting as granulomatous inflammation and vasculitis. Despite the species similarity to Encephalitozoon cuniculi, which causes ocular, neurologic, and renal pathology in
Vanessa Raphtis, Megan Roeder, Augusto Jimenez‐Romero, Danielle Meritet, Kelli Chan, Sarah Ozawa, Michala de Linde Henriksen   +6 more
wiley   +1 more source

Spontaneous Regression of a Verrucous Venous Malformation Associated with a Previously Undescribed MAP3K3 Variant. [PDF]

Acta Derm Venereol
Diociaiuti A, Bellacchio E, Cesario C, Rossi S, Zambruno G, El Hachem M.   +5 more
europepmc   +1 more source

Penile Pseudoepitheliamatous Hyperkeratosis balanitis: A case report and review in Assiut university urology department 2021

, 2021
Abdelrahman Mohamed Abdelkader Osman, Mahmoud Khalil, Mohamed Abdullah Morsy ElGammal, Dalia Elsers   +3 more
openalex   +1 more source

Nail Disease in Psoriatic Arthritis: Distal Phalangeal Bone Edema Detected by Magnetic Resonance Imaging Predicts Development of Onycholysis and Hyperkeratosis

Journal of Rheumatology, 2012
N. Dalbeth, K. Pui, Maria Lobo, A. Doyle, Peter B B Jones, W. Taylor, F. McQueen   +6 more
semanticscholar   +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

Epidermolytic hyperkeratosis with a rare digital contracture

, 2007
Sudip Das, Alok Kumar Roy, Chinmoy Kar, Arunasis Maiti   +3 more
openalex   +1 more source

Hyperkeratosis in potentially malignant disorder management – ‘guilty… until proven innocent!’ [PDF]

, 2019
StJohn Crean, Peter Thomson
openalex   +1 more source

Pigmented Aqua-Exacerbated Symmetrical Acral Hyperkeratosis

, 2021
M. Bandhala Rajan, Abhishek Bhardwaj, Sudeep Khera, Varun Rajagopal   +3 more
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