Results 31 to 40 of about 9,316 (182)

EPIDERMOLYSIS BULLOSA PRURIGINOSA, A CASE REPORT AND REVIEW OF THE LITERATURE

Journal of IMAB, 2020
Purpose: Epidermolysis bullosa pruriginosa (EBP) is a rare clinical subtype of inherited Epidermolysis bullosa dystrophica (EBD). It is characterized by severe itching and hypertrophic papules affecting the extensor surfaces of the extremities ...
Ivelina Yordanova, Mariya Binova, Preslav Vasilev, Milen Karaivanov, Dimitar Gospodinov   +4 more
doaj   +1 more source

Epidermólise bolhosa distrófica recessiva mitis: relato de caso clínico Recessive dystrophic epidermolysis bullosa mitis: case report

Anais Brasileiros de Dermatologia, 2005
As epidermólises bolhosas são dermatoses bolhosas congênitas que levam à formação de bolhas espontaneamente ou após trauma. São reconhecidos três grupos de da doença, de acordo com o segundo consenso internacional: simples, juncional e distrófica.
Thaiz Gava Rigoni Gürtler, Lucia Martins Diniz, João Basilio de Souza Filho   +2 more
doaj   +1 more source

Epidermolysis bullosa: how social support affects quality of life

, 2018
Measuring quality of life has become an increasingly important method of evaluating the effect of health and social care interventions. The rare genetic condition epidermolysis bullosa is known to have a deep social impact on people’s quality of life ...
Butterworth, Sondra, Martin, Kate, Mason-Whitehead, Elizabeth, Mitchell, Andrew E. P.   +3 more
core   +2 more sources

Epidermólise bolhosa distrófica pruriginosa: relato de caso Epidermolysis bullosa pruriginosa: case report

Anais Brasileiros de Dermatologia, 2005
A epidermólise bolhosa distrófica pruriginosa é doença genética rara cujo padrão de herança ainda não está bem estabelecido na literatura. O defeito genético, que envolve a codificação do colágeno tipo VII, está localizado no braço curto do cromossomo 3,
Márcio José Silva de Souza, Carla Andréa Avelar Pires, Karine Keila de Sousa Vieira, Mario Fernando R. de Miranda, Deborah Aben-Athar Unger   +4 more
doaj   +1 more source

Mogućnosti prevencije oralnih oboljenja kod dece obolele od epidermolysis bullosa dystrophica [PDF]

, 2017
Epidermolysis bullosa (EB) is a genetic multisystem, genetically and clinically heterogeneous group of diseases characterized by extreme sensitivity of the skin and mucous membranes, where blisters and erosions occur after minor mechanical trauma ...
Čolović, Aleksandra
core   +1 more source

Surgical management of squamous cell carcinoma arising in patients affected by epidermolysis bullosa: a comparative study

, 2020
International Wound Journal, Volume 17, Issue 2, Page 519-521, April 2020.
Alessia Paganelli, Camilla Reggiani, Chiara Fiorentini, Mario Lando, Anna M. Cesinaro, Cristina Magnoni   +5 more
wiley   +1 more source

Patient-generated evidence in Epidermolysis Bullosa (EB): Development of a questionnaire to assess the Quality of Life [PDF]

, 2021
Epidermolysis Bullosa (EB) is a group of genetic conditions that cause fragile and blistering skin. Although there are different types of EB, which differ in severity, their signs and symptoms overlap.
Gianluca Tadini, Mariani, Paolo, Carlotta Galeone, Laura Benedan, Paolo Mariani, Galeone, Carlotta, El Hachem, May, Cinzia Pilo, Benedan, Laura, May El Hachem, Pilo, Cinzia, Tadini, Gianluca   +11 more
core   +1 more source

Nevo da epidermólise bolhosa: aspectos clínicos, dermatoscópicos e histológicos em um caso de portador da forma distrófica recessiva Epidermolysis bullosa nevi: clinical, dermatoscopical and histological features in a case of recessive dystrofic form

Anais Brasileiros de Dermatologia, 2011
As lesões melanocíticas adquiridas podem apresentar aspecto clínico não-usual em pacientes portadores de epidermólise bolhosa hereditária. Essas lesões são conhecidas como "nevos EB" e, muitas vezes, constituem um desafio diagnóstico ao dermatologista ...
Juliana Nakano de Melo, Priscila Yoshie Teruya, Maria Cecília Rivitti Machado, Neusa Sakai Valente, Mirian Nacagami Sotto, Zilda Najjar Prado de Oliveira   +5 more
doaj   +1 more source

Elements of morphology: Standard terminology for the teeth and classifying genetic dental disorders

American Journal of Medical Genetics Part A, Volume 179, Issue 10, Page 1913-1981, October 2019., 2019
Abstract Dental anomalies occur frequently in a number of genetic disorders and act as major signs in diagnosing these disorders. We present definitions of the most common dental signs and propose a classification usable as a diagnostic tool by dentists, clinical geneticists, and other health care providers.
Muriel de La Dure‐Molla, Benjamin Philippe Fournier, Maria Cristina Manzanares, Ana Carolina Acevedo, Raoul C. Hennekam, Lisa Friedlander, Marie‐Laure Boy‐Lefèvre, Stephane Kerner, Steve Toupenay, Pascal Garrec, Brigite Vi‐Fane, Rufino Felizardo, Marie‐Violaine Berteretche, Laurence Jordan, François Ferré, François Clauss, Sophie Jung, Myriam de Chalendar, Sebastien Troester, Marzena Kawczynski, Jessica Chaloyard, International Group of Dental Nomenclature, Marie Cécile Manière, Ariane Berdal, Agnès Bloch‐Zupan   +24 more
wiley   +1 more source

Acquired syndactyly in epidermolysis bullosa dystrophica

BMJ Case Reports, 2009
The index case, a resident of Chandigarh, presented at 2 years age with history of blistering skin lesions from day 2 of life. The blisters contained clear or blood-tinged fluid, 7–10 lesions developed every week, and these ruptured spontaneously, and did not involve cheeks, chin, soles or genitalia.
Inusha, Panigrahi, Ketan, Kulkarni, Devi, Dayal   +2 more
openaire   +3 more sources