Results 161 to 170 of about 39,840 (293)

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

Incidencia de la eritroleucoplasia en la cavidad bucal Incidence of erythroleukoplakia in the oral cavity

Medisan, 2012
Se efectuó un estudio descriptivo y transversal de 20 mujeres y hombres mayores de 19 años, adictos al tabaco, atendidos en la consulta estomatológica del Policlínico de Especialidades del Hospital Provincial Docente "Saturnino Lora Torres" de Santiago ...
Gladys Aída Estrada Pereira, Maricel Márquez Filiú, Eugenia González Heredia   +2 more
doaj  

Anatomopathological Characterization of the Main Ocular Lesions in Green Turtles (Chelonia mydas) Along the Northern Coast of Bahia, Brazil

Veterinary Ophthalmology, EarlyView.
ABSTRACT Objective This study aimed to identify and report ophthalmic and adnexal diseases found in specimens of the Green sea turtle (Chelonia mydas). Animal Studied and Procedures Thirty‐nine animals stranded on the beaches of the north coast of Bahia, Brazil were submitted to necropsy.
Danielle Nascimento Silva, José Luís Catão‐Dias, Wendell Marcelo de Souza Perinotto, Matheus Vilardo Loés Moreira, Nayone Lantyer‐Araujo, Pedro Enrique Navas Suárez, Gustavo Rodamilans Macedo, Thaís Pires, Arianne Pontes Oriá, Alessandra Estrela‐Lima   +9 more
wiley   +1 more source

Hyperkeratosis Follicularis et Parafollicularis in Cutem Penetrans (Kyrle)

, 1947
James R. Simpson
openalex   +2 more sources

The HRAS Variant c.175G>A (p.Ala59Thr) Causes a Predominantly Ectodermal Phenotype Lacking Classic Costello Syndrome Features

American Journal of Medical Genetics Part A, Volume 200, Issue 2, Page 407-418, February 2026.
ABSTRACT Costello syndrome (CS) is a rare dominant HRAS RASopathy characterized by curly hair, cardiac abnormalities, craniofacial anomalies, and developmental delay. HRAS codon 58, 59, and 60 variants are associated with milder phenotypes. We describe a three‐generation family with a previously unreported heterozygous HRAS variant c.175G>A (p.Ala59Thr)
Nikole Rautiainen, Eveliina Brandt, Kaisa Kettunen, Outi Elomaa, Sirpa Kivirikko, Leila Jeskanen, Katriina Lappalainen, Nelli Sjöblom, Juha Kere, Katariina Hannula‐Jouppi, Liisa Harjama   +10 more
wiley   +1 more source

Assessing the use of dupilumab in a pediatric patient with bullous congenital ichthyosiform erythroderma

JAAD Case Reports, 2023
Nouf Almuhanna, MD, Anwar R. Alrashidi, MD, Esraa A. Shaheen, MD, Yasmeen Alanazi, MD, Abdulrahman Alfawzan, MD, Raghad Alharthi, MD, Faris A. Alhomida, MD   +6 more
doaj   +1 more source

Dermoscopy of Lichen Planus Follicularis Tumidus: A Case Report With Pattern Analysis and Literature Review

Clinical Case Reports, Volume 14, Issue 2, February 2026.
ABSTRACT Lichen planus follicularis tumidus (LPFT) is a rare variant of lichen planus presenting as erythematous to violaceous plaques with significant follicular involvement, most commonly in the retroauricular area. We report a case demonstrating a novel dermoscopic pattern reminiscent of a follicular galaxy, composed of variably sized comedo‐like ...
Vahidehsadat Azhari, Mina Saber
wiley   +1 more source

Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report

Clinical Case Reports, Volume 14, Issue 2, February 2026.
ABSTRACT Monilethrix is a rare genetic disorder characterized by sparse, brittle hair, primarily affecting the scalp, although it may also affect other parts of the body. Trichorrhexis nodosa (TN) is another hair shaft disorder characterized by brittle and fragile hair shafts. Concurrence of monilethrix and TN is exceedingly rare.
Yasamin Dehghan, Mozhdeh Sepaskhah
wiley   +1 more source

Relationship between milk somatic cell count and teat end hyperkeratosis in dairy cows [PDF]

, 2014
Ivana Davidov, Mihajlo Erdeljan, Zorana Kovačević, Miodrag Radinović   +3 more
openalex   +1 more source

Unilateral Nevoid Hyperkeratosis of the Nipple and Areola: A Case Report of a Rare Entity. [PDF]

Cureus
Shamsaldeen F, Mosbeh A, Albazali A.
europepmc   +1 more source