Oral Manifestations of Epidermolysis Bullosa in a Newborn: a Case Report of Photobiomodulation Treatment

Author(s):  
Gabriela Costa ◽  
Gabriela De Almeida Camassola ◽  
Nathália Alves Paz Maciel ◽  
Michelli Flores ◽  
Felipe Corá ◽  
...  
1969 ◽  
Vol 40 (7) ◽  
pp. 431-434 ◽  
Author(s):  
Bernard P. Levy ◽  
Charles M. Reeve ◽  
Robert R. Kierland

Author(s):  
Marjorie Das Posses Bridi ◽  
Renata Caroline Wanderley Nobre ◽  
Rosany Larissa Brito De Oliveira ◽  
Valtuir Barbosa Felix ◽  
Andréia Barbosa Da Silva ◽  
...  

2018 ◽  
Vol Volume 5 ◽  
pp. 17-21
Author(s):  
Caroline Fife ◽  
Raphael Yaakov ◽  
Thomas Serena

2000 ◽  
Vol 14 (4) ◽  
pp. 211-213 ◽  
Author(s):  
Zerrìn ÖzkÖse ◽  
Hülya Çelebì ◽  
Kutluk Pampal ◽  
Bìllur Altuntaş

2011 ◽  
Vol 2011 ◽  
pp. 1-4
Author(s):  
Gaurav Sharma ◽  
Archna Nagpal

Nevus of Ota, a dermal melanocytic nevus, is rare in the Indian subcontinent. It presents as a brown, blue, or gray patch on the face and is within the distribution of the ophthalmic and maxillary branches of the trigeminal nerve. The oral cavity is infrequently involved in nevus of Ota. Only 11 cases have been documented in the English literature. We report a rare case of intraoral nevus of Ota in a 22-year-old male patient. This paper focuses on the differential diagnosis of oral manifestations of nevus of Ota to assist in proper followup to avert malignant transformation.


PEDIATRICS ◽  
1986 ◽  
Vol 78 (1) ◽  
pp. 172-174
Author(s):  
MARGARET A. KENNA ◽  
SYLVAN E. STOOL ◽  
SUSAN B. MALLORY

Epidermolysis bullosa is a rare genetically determined, dermatologic disease in which minor trauma causes blister formation.1 A new variant of hereditary epidermolysis bullosa, generalized atrophic benign epidermolysis bullosa, junctional form, has been recently reported.2 Airway involvement has not been a notable feature of this disease. We report the first case of an infant having benign junctional epidermolysis bullosa with laryngeal involvement. CASE REPORT An 11-month-old white boy with known junctional epidermolysis bullosa and mild stridor since birth was referred by his dermatologist for increasing stridor of 24 hours duration. He was initially thought to have croup; however, conservative treatment with mist and racemic epinephrine did not improve his symptoms.


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