Results 131 to 140 of about 9,316 (182)

Laryngeal stenosis in epidermolysis bullosa dystrophica

Auris Nasus Larynx, 2009
Epidermolysis bullosa dystrophica is a rare hereditary skin disease of infancy in which minor trauma causes blister formation. We report a rare case of epidermolysis bullosa dystrophica (recessive) with a stenosis of the larynx due to epiglottic deformity. We performed a tracheotomy, and we detained a trachea aperture in the long term this time.
Katsuhisa Ikeda, Fumihiko Matsumoto, Masayuki Furukawa   +2 more
exaly   +3 more sources

Epidermolysis bullosa dystrophica with urinary tract involvement

Journal of Pediatric Surgery, 1984
A case of epidermolysis bullosa dystrophica ( EBD ), neonatally corrected atresia of the pylorus and early infantile development of urinary tract manifestations is reported. Owing to misinterpretation of radiological findings, instrumental treatment of the urethra was employed. It resulted in complete and permanent obliteration of the lumen.
O, Eklöf, K, Parkkulainen
exaly   +3 more sources

Clinical manifestations of epidermolysis bullosa dystrophica

Digestive Diseases and Sciences, 1981
Dennis M Balfe, R E Koehler
exaly   +3 more sources

Severe osteoporosis treated with teriparatide in a patient affected by recessive epidermolysis bullosa dystrophica

Osteoporosis International, 2010
In this work, we describe the clinical and instrumental results of our experience, the first reported in the literature, of the administration of teriparatide to treat severe osteoporosis secondary to epidermolysis bullosa.
Biagio Moretti, Angela Notarnicola, L Moretti   +2 more
exaly   +2 more sources

A case of congenital pyloric atresia with dystrophic epidermolysis bullosa

Pediatric Surgery International, 2014
Pyloric atresia with epidermolysis bullosa (EB) dystrophica is a rare entity that may not be immediately recognized. We describe the fourth confirmed case of pyloric atresia associated with the dystrophic subtype of EB diagnosed by standard pathologic ...
Henri R Ford, Scott S Short, Christa N Grant   +2 more
exaly   +2 more sources

Epidermolysis bullosa dystrophica

1990
Epidermolysis bullosa dystrophica (EBD) is a heterogeneous group of inherited mechanobullous diseases that produce separation in the deep portion of the basement membrane zone beneath the lamina densa (dermolytic separation) [1, 2] (Figure 16.1). Dystrophic scarring results from repeated blistering and serves as a clinical marker of these diseases ...
Robert A. Briggaman, Eugene A. Bauer
openaire   +1 more source

Epidermolysis Bullosa Dystrophica Inversa in a Child

Pediatric Dermatology, 1990
Abstract: A 4‐year‐old child with dystrophic epidermolysis bullosa inverse is described. Clinical features were blistering of the skin, erosions, scarring and milia formation. The areas involved included the trunk, with preference for the axillary and inguinal folds, the neck and sacral area, and proximal extremities.
Bruckner-Tuderman L, Pfaltz M, Schnyder UW   +2 more
openaire   +3 more sources

Esophageal involvement in epidermolysis bullosa dystrophica

American Journal of Roentgenology, 1983
The clinical and radiographic findings in four cases of epidermolysis bullosa dystrophica of the esophagus are presented. The patients were 5-67 years old. All had typical skin lesions and dysphagia. The most impressive radiographic finding was bulla formation in virtually any part of the esophagus. The bullae would resolve or ulcerate.
J M, Tishler, S Y, Han, C A, Helman
openaire   +2 more sources

Epidermolysis Bullosa Dystrophica in Children

Radiology, 1968
Epidermolysis bullosa is a rare hereditary skin disease, in which slight trauma disrupts the cohesion between the epidermis and the dermis, resulting in the formation of vesicles, bullae, and ulcers. Sorsby (4) described three principal types of this disease.
M H, Becker, C A, Swinyard
openaire   +2 more sources