Results 91 to 100 of about 1,088 (130)

Epidermolysis bullosa dystrophica - prezentacja przypadku

Pediatria Polska, 2002
Pindycka-Piaszczyńska, M, Behrendt, J, Kuhny, D, Kułagowska-Timberman, E, Filipowska, B   +4 more
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Epidermolysis Bullosa Pruriginosa Treated With Upadacitinib.

JAMA Dermatol
Zhang Z, Lin Z.
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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.
Takuo, Haruyama, Masayuki, Furukawa, Fumihiko, Matsumoto, Kenji, Kawano, Katsuhisa, Ikeda   +4 more
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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
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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
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Epidermolysis Bullosa Dystrophica With Urinary Tract Involvement

Journal of Urology, 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
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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
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Esophageal Epidermolysis Bullosa Dystrophica?

Annals of Internal Medicine, 1975
Excerpt To the editor: The discussion of gastrointestinal manifestations in epidermolysis bullosa dystrophica (recessive) by Orlando and colleagues (Ann Intern Med81:203-206, 1974) was most informa...
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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.
L, Bruckner-Tuderman, M, Pfaltz, U W, Schnyder   +2 more
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Epidermolysis Bullosa Dystrophica: Report of Two Cases

The Journal of the American Dental Association, 1972
Oral conditions of patients with an advanced form of epidermolysis bullosa dystrophica, a rare disease of unknown cause, include poorly calcified teeth and hypoplastic enamel. Generally, the patients cannot use good oral hygiene techniques because of trauma to the gingival tissues.
E F, Howden, T R, Oldenburg
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