Results 31 to 40 of about 144 (122)

Incontinência pigmentar ligada ao X ou síndrome de Bloch-Sulzberger: relato de um caso X-linked incontinentia pigmenti or Bloch-Sulzberger syndrome: a case report

Anais Brasileiros de Dermatologia, 2010
A incontinência pigmentar é uma genodermatose rara, ligada ao X, que afeta, principalmente, neonatos do sexo feminino. As manifestações cutâneas são as mais prevalentes, e ocorrem em quatro fases bem distintas. Lactente feminina com lesões vesicobolhosas
Marcela A. C. Pereira, Lismary A. de F. Mesquita, Anelise R. Budel, Carolina S. P. Cabral, Amanda de S. Feltrim   +4 more
doaj   +1 more source

A Neutral Comparison of Multivariate Hypothesis Tests for Parallel Group Designs in Rare Disease Settings

Statistics in Medicine, Volume 45, Issue 20-22, September 2026.
ABSTRACT Multivariate endpoints are increasingly used in clinical studies on rare diseases, where sample sizes tend to be small and distributional assumptions are often violated. In such settings, commonly applied parametric multivariate methods, such as classical MANOVA approaches, may suffer from inflated type‐I error or reduced statistical power ...
Martin Geroldinger, Martin Laimer, Verena Wally, Johann W. Bauer, Georg Zimmermann   +4 more
wiley   +1 more source

Terapia fotodinâmica para tratamento de múltiplas lesões no couro cabeludo na síndrome do nevobasocelular: relato de caso Photodynamic therapy for treatment of multiple lesions on the scalp in nevoid basal cell carcinoma syndrome: case report

Anais Brasileiros de Dermatologia, 2010
A terapia fotodinâmica é uma alternativa eficaz de tratamento para neoplasias cutâneas não melanoma e tem como princípio a utilização de substâncias fotossensibilizantes que, após serem irradiadas com uma fonte de luz de comprimento de onda adequado ...
Daniela Rezende Neves, Daniel Gontijo Ramos, Geraldo Magela Magalhães, Rogério da Costa Rodrigues, Joana Barbosa Alves de Souza   +4 more
doaj   +1 more source

Long‐Term Efficacy and Safety of Oleogel‐S10 (Birch Triterpenes) for Pediatric Patients With Epidermolysis Bullosa

Pediatric Dermatology, Volume 43, Issue 5, Page 1111-1119, September/October 2026.
ABSTRACT Background/Objectives Pediatric patients with epidermolysis bullosa (EB) experience lifelong complications, and wound healing is an important treatment goal. In the phase III EASE study (NCT03068780), Oleogel‐S10 accelerated wound healing in EB.
Eli Sprecher, Mauricio Torres‐Pradilla, Maria Florencia Fernandez, Christine Bodemer, Anna L. Bruckner, Silvia Maria de Macedo Barbosa, Andrea Diociaiuti, Anna E. Martinez, Francis Palisson, Miloš Nikolić, Asunción Vicente, Raúl de Lucas, Noemi Toiber Temin, Sandra Löwe, Johannes S. Kern, Dédée F. Murrell, the EASE Study Group   +16 more
wiley   +1 more source

Advanced Imaging Techniques for Early in‐Vivo Discrimination of Fibrofolliculomas in Birt‐Hogg‐Dubé Syndrome

Skin Research and Technology, Volume 32, Issue 9, September 2026.
ABSTRACT Background Birt‐Hogg‐Dubé syndrome (BHDS) is a rare genetic tumor syndrome characterized by cutaneous fibrofolliculoma and trichodiscomas, lung bullae with an elevated risk of spontaneous pneumothorax and renal cell cancer. Objectives Due to rareness of the disease, clinical symptoms and cutaneous manifestations are often misjudged, resulting ...
Maximilian Deußing, Daniela Hartmann, Pontus Mertsch, Charlotte Gust, Michael J. Flaig, Marlene Reithmair, Julia Hoefele, Elke C. Sattler   +7 more
wiley   +1 more source

Culturally Safe and Decentralised Care: Patient Experiences of a Dermatology Clinic Embedded in an Aboriginal and Torres Strait Islander Primary Health Care Service

Australasian Journal of Dermatology, Volume 67, Issue 5, Page 294-300, August 2026.
ABSTRACT Background Skin disease is a major cause of morbidity in Australia and a leading reason for primary care visits. Aboriginal and Torres Strait Islander peoples experience a disproportionate burden of skin conditions but face barriers to accessing culturally safe specialist services.
Nikhil Dwivedi, Nicholas Van Rooij, Geoffrey Spurling, Claudette (Sissy) Tyson, Sonya Egert, Erin McMeniman, Noel Hayman   +6 more
wiley   +1 more source

Doença de Dowling-Degos: apresentação clínica e histopatológica clássica Dowling-Degos disease: classic clinical and histopathological presentation

Anais Brasileiros de Dermatologia, 2011
A doença de Dowling-Degos é uma genodermatose rara que consiste numa desordem pigmentar reticulada. Caracteriza-se pela presença de máculas hiperpigmentadas nas regiões flexurais com distribuição em rede; lesões tipo comedão no dorso e na região cervical;
Carolina Cotta Zimmermann, Deborah Sforza, Priscila Marques de Macedo, Luna Azulay-Abulafia, Maria de Fatima G. S Alves, Sueli Coelho da S Carneiro   +5 more
doaj   +1 more source

Epidermolysis Bullosa Classification and Current Approach to Diagnosis

Pediatric Dermatology, Volume 43, Issue S2, Page 5-15, August 2026.
ABSTRACT Epidermolysis bullosa (EB) is a heterogeneous group of rare genodermatoses marked by skin fragility and bullae formation induced by minor trauma. Pathologic variants in at least 21 genes are associated with EB, grouped into four major subtypes based predominantly on the plane of cleavage within the skin.
Hannah E. Mumber, Marissa J. Perman
wiley   +1 more source

FEOCROMOCITOMA E NEUROFIBROMATOSE 1

Revista da Sociedade Portuguesa de Dermatologia e Venereologia, 2014
Introdução: Feocromocitomas são tumores originários de células cromafins do sistema simpato-adrenal. As suas manifestações clínicas são múltiplas e diversificadas, função do perfil secretório variável de múltiplos compostos, incluindo catecolaminas ...
Rui Tavares-Bello, Mafalda Marcelino, Ema L. Nobre, Luís Lopes, Carlos Lopes, João Jácome de Castro   +5 more
doaj   +1 more source

Encorafenib‐associated acantholytic dermatosis in collision with eccrine squamous syringometaplasia

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Francisco Meraz‐Torres, Gabi Handgretinger, Andreas Meiwes, Derya Durak, Joana Schroth, Stephan Forchhammer   +5 more
wiley   +1 more source