Results 31 to 40 of about 762 (161)

High-fluence 1064nm Q-switched Nd:YAG laser treatment for ectopic Mongolian spot

Journal of Dermatological Treatment, 2023
Q-switched neodymium-yttrium aluminum-garnet (Q-switched Nd:YAG) laser has been reported as an effective treatment for nevus of Ota and acquired bilateral nevus of Ota-like macules (ABNOM). Data on ectopic Mongolian spots have rarely been reported.
Jun-Oh Shin, Dongyoung Roh, Kihyuk Shin, Hoon-Soo Kim, Byung-Soo Kim, Moon-Bum Kim, Hyun-Chang Ko   +6 more
doaj   +1 more source

Secondary Glaucoma Resulting From Choroidal Melanoma in a Patient With Congenital Nevus of Ota. [PDF]

Case Rep Ophthalmol Med
Purpose First, to report nevus of Ota accompanying ocular melanoma in Thai patients. Second, to report angle‐closure glaucoma as a presentation secondary to ocular melanoma along with a pathological report giving insight into the pathophysiology of secondary glaucoma in uveal melanoma.
Petchyim S, Pongrujikorn S, Lizarondo FPJ, Manuskiatti W.   +3 more
europepmc   +2 more sources

A 1‐year and 4‐month‐old child with mucopolysaccharidoses type II: A clinical case report from Ethiopia

Clinical Case Reports, 2021
Mucopolysaccharidoses (MPSs) are a class of lysosomal storage disorders resulting in progressive disease manifestations and are caused by pathogenic variants in genes coding for enzymes needed to degrade glycosaminoglycans.
Solomie Jebessa Deribessa, Mekdes Endale Bisrat, Zewdu Terefework, Shane C. Quinonez   +3 more
doaj   +1 more source

What the skin of 341 premature newborns says - a transversal study

Jornal de Pediatria, 2023
Objectives: Determine the frequency of dermatological diagnoses in preterm newborns up to 28 days of life and associated perinatal factors. Method: a cross-sectional analytical study with a convenience sample and prospective data collection, was ...
Danielle Arake Zanatta, Vânia Oliveira Carvalho, Regina Paula Guimarães Vieira Cavalcante da Silva   +2 more
doaj   +1 more source

Nevus of Ota – an intraoral presentation: a case report

Journal of Medical Case Reports, 2019
Background Nevus of Ota or “oculodermal melanocytosis” is a rare congenital hamartoma of dermal melanocytes causing a blue-gray hyperpigmentation of the eye and surrounding structures. The condition, originally described by Ota and Tanino in 1939, mainly
Jennifer Maguire, Deborah Holt
doaj   +1 more source

Epidemiología y factores predisponentes de los hallazgos dermatológicos en neonatos de Uruguay

Actas Dermo-Sifiliográficas, 2021
Resumen: Introducción: La piel es fundamental en la transición de la vida intrauterina a la extrauterina. El recién nacido presenta cambios fisiológicos, siendo frecuente observar hallazgos cutáneos benignos y transitorios que varían según las ...
M.K. De María, K.M. Borda, V.N. Arretche, N. Gugelmeier, R. Mombelli, A.V. de los Santos, M.A. Acosta, M. Álvarez, G.L. Pose, D. Borbonet, M.A. Martínez   +10 more
doaj   +1 more source

Imatinib-Induced Acquired Dermal Melanocytosis [PDF]

SKIN The Journal of Cutaneous Medicine, 2021
Background: Imatinib, a tyrosine kinase inhibitor targeting bcr-abl, c-Kit, and PDGF receptors-alpha and beta, is commonly used to treat GI stromal tumors and hematologic malignancies. Hyperpigmentation is a known side-effect of imatinib, with intradermal hemosiderosis being the most common histologic finding.
Anna Eversman, Sakeena Fatima, Kord Honda, Mara Beveridge   +3 more
openaire   +1 more source

Dermatological Characteristics in a Cohort of Patients with Mucopolysaccharidosis from Southwestern Colombia [PDF]

Journal of Inborn Errors of Metabolism and Screening
Background: Mucopolysaccharidoses (MPS) are rare lysosomal storage disorders characterized by glycosaminoglycan accumulation and multisystem involvement, including underreported dermatological features.
Johan Conquett Huertas, Winnie Celorio, Jose Maria Satizabal, Lina Moreno Giraldo   +3 more
doaj   +2 more sources

Prevalence and characterization of neonatal skin disorders in the first 72 h of life,

Jornal de Pediatria, 2017
Objective: To determine the prevalence of neonatal dermatological findings and analyze whether there is an association between these findings and neonatal and pregnancy characteristics and seasonality. Methods: Newborns from three maternity hospitals in
Flávia Pereira Reginatto, Damie DeVilla, Fernanda M. Muller, Juliano Peruzzo, Letícia P. Peres, Raquel B. Steglich, Tania F. Cestari   +6 more
doaj   +3 more sources

Mucopolysaccharidosis Type I

Diagnostics, 2020
Mucopolysaccharidosis type I (MPS I) is caused by the deficiency of α-l-iduronidase, leading to the storage of dermatan and heparan sulfate. There is a broad phenotypical spectrum with the presence or absence of neurological impairment.
Francyne Kubaski, Fabiano de Oliveira Poswar, Kristiane Michelin-Tirelli, Ursula da Silveira Matte, Dafne D. Horovitz, Anneliese Lopes Barth, Guilherme Baldo, Filippo Vairo, Roberto Giugliani   +8 more
doaj   +1 more source