Results 1 to 10 of about 1,088 (130)

Clinical management for epidermolysis bullosa dystrophica [PDF]

Journal of Applied Oral Science, 2008
Epidermolysis bullosa (EB) consists of a group of genetic hereditary disorders in which patients frequently present fragile skin and mucosa that form blisters following minor trauma.
Thais M. Oliveira, Vivien T. Sakai, Liliani A. Candido, Salete M. B. Silva, Maria Aparecida A. M. Machado   +4 more
doaj   +7 more sources

Role of regional anaesthesia in a patient with epidermolysis bullosa dystrophica for emergency surgery [PDF]

Indian Journal of Anaesthesia, 2021
Thirumurugan Arikrishnan, Deepak Chakravarthy, Vijayanthi Vijayan, Gnanasekaran Srinivasan   +3 more
doaj   +2 more sources

Epidermolysis bullosa dystrophica inversa: case report of a novel genetic mutation, involving a rare genodermatoses [PDF]

Indian Dermatology Online Journal, 2023
Abhijit S Chakraborty, Rashmi Agarwal, Pellakuru Preethi, B S Chandrashekar   +3 more
doaj   +2 more sources

Acquired syndactyly in epidermolysis bullosa dystrophica.

BMJ Case Rep, 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.
Panigrahi I, Kulkarni K, Dayal D.
europepmc   +4 more sources

Scrape to Nail the Diagnosis: A “Mitey” Challenge in an Erythroderma [PDF]

Journal of Clinical and Diagnostic Research, 2023
Norwegian (crusted) scabies is a highly contagious form of scabies which can evolve into erythroderma at times. We herein report a case of a 29-year-old male patient, an established case of epidermolysis bullosa dystrophica (EBD), presented to us with ...
S Praveen Kumar, TK Sumathy, AL Shyam Prasad, Archana Lakshman   +3 more
doaj   +1 more source

Oral and perioral soft tissue lesions and oral functions in patients with dystrophic epidermolysis bullosa [PDF]

Vojnosanitetski Pregled, 2022
Background/Aim. Dystrophic epidermolysis bullosa (DEB) is characterized by distinct systemic and skin changes, as well as numerous oral manifestations. The aim of the study was to examine oral and perioral soft tissues and oral functions in DEB patients ...
Čolović Aleksandra, Jovičić Olivera, Mandinić Zoran, Mandić Jelena, Juloski Jelena   +4 more
doaj   +1 more source

Epidermolysis bullosa: A report of three cases with novel heterozygous deletions in PLEC and homozygous non sense mutations in COL7A1 genes

Indian Journal of Dermatology, 2022
Epidermolysis bullosa (EB) is a group of rare inherited conditions that results in blistering of the skin and mucous membranes. Mutations in the PLEC gene cause epidermolysis bullosa simplex (EBS).
Sunitha Tella, Shehnaz Sultana, Sujatha Madireddy, Pratibha Nallari, Venkateshwari Ananthapur   +4 more
doaj   +1 more source

Oral health status in children with inherited dystrophic epidermolysis bullosa [PDF]

Vojnosanitetski Pregled, 2017
Background/Aim. Epidermolysis bullosa is a group of rare, genetic connective tissue diseases that cause blisters in the skin and mucosal membranes.
Čolović Aleksandra, Jovičić Olivera, Stevanović Radoje, Ivanović Mirjana   +3 more
doaj   +1 more source

Pretibial dystrophic epidermolysis bullosa [PDF]

Anais Brasileiros de Dermatologia, 2017
Epidermolysis bullosa is a group of mechano-bullous genetic disorders caused by mutations in the genes encoding structural proteins of the skin. Dystrophic epidermolysis bullosa is caused by mutations in the COL7A1 gene encoding collagen VII, the main ...
Elisabeth de Albuquerque Cavalcanti Callegaro, Flavio Nappi, Rosana Lazzarini, Rute Facchini Lellis   +3 more
doaj   +1 more source

Otorhinolaryngological and esophageal manifestations of epidermolysis bullosa

Brazilian Journal of Otorhinolaryngology, 2008
Summary: Epidermolysis bullosa (EB) is a group of skin diseases with different clinical manifestations and varied inheritance patterns. Blisters may appear spontaneously or following minimal trauma to the skin or mucosa.
Rodrigo Santana Fantauzzi, Mariana Oliveira Maia, Flávia Coelho Cunha, Rodrigo Vidal Simões, Denise Utsch Gonçalves, Amélio Ferreira Maia   +5 more
doaj   +1 more source