Results 161 to 170 of about 2,763 (196)

Junctional Epidermolysis Bullosa of the Larynx

Pediatrics, 1987
To the Editor.— The article by Kenna et al (Pediatrics 1986;78:172-174) points out the complication of respiratory compromise secondary to laryngeal involvement in junctional epidermolysis bullosa. Junctional epidermolysis bullosa, a mechanobullous disorder with autosomal recessive inheritance, has been associated with not only skin ...
A, Gonzalez, L, Schachner, M, Miller
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Cicatricial junctional epidermolysis bullosa

Journal of the American Academy of Dermatology, 1994
cinorna mimicking zoster sine herpete. Arch Dermatol 1986;122: 1357-8. 8. Fetter TR, Bogaev JH, McCuskey B, et al. Carcinomaof the bladder: sites of metastasis. J Urol 1959;81 :746-8. 9. McDonald JH, Heckel NJ, Kretchemer HL. Cutaneous metastases secondary tocarcinoma of the urinarybladder. Arch Derrnatol Syphilol 1950;61 :210-2. 10.
Jonkman, MF, de Jong, MCJM, van der Meer, JB   +2 more
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Herlitz Junctional Epidermolysis Bullosa

Dermatologic Clinics, 2010
Junctional epidermolysis bullosa type Herlitz (JEB-H) is the autosomal recessively inherited, more severe variant of "lucidolytic" JEB. Characterized by generalized, extensive mucocutaneous blistering at birth and early lethality, this devastating condition is most often caused by homozygous null mutations in the genes LAMA3, LAMB3, or LAMC2, each ...
Martin, Laimer, Christoph M, Lanschuetzer, Anja, Diem, Johann W, Bauer   +3 more
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Non-Herlitz Junctional Epidermolysis Bullosa

Dermatologic Clinics, 2010
Non-Herlitz junctional epidermolysis bullosa (nH JEB) is characterized by generalized blisters that predominate in sites exposed to friction, trauma, or heat. Whereas infants and children with nH JEB often appear to resemble patients with other forms of EB, adults with this disorder typically display atrophic scars, hypopigmentation, or ...
Kim B, Yancey, Helmut, Hintner
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Eye Involvement in Junctional Epidermolysis Bullosa

Archives of Ophthalmology, 1989
The ocular findings in a group of five patients with the nonlethal form of junctional epidermolysis bullosa are presented. A history of recurrent corneal erosion and the presence of corneal scarring were the most common findings. We discuss the possible mechanisms of the ocular changes and describe how the recent application of monoclonal antibody ...
P J, McDonnell, O M, Schofield, D J, Spalton, R A, Eady   +3 more
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Autosomal dominant junctional epidermolysis bullosa

British Journal of Dermatology, 2009
Epidermolysis bullosa (EB) encompasses a heterogeneous group of inherited skin disorders associated with trauma-induced blistering. The junctional forms of EB (JEB), Herlitz JEB, non-Herlitz JEB and JEB associated with pyloric atresia have all been attributed to autosomal recessive inheritance. We describe a 7-year-old girl with defective dental enamel,
Almaani, N., Liu, L., Dopping-Hepenstal, P. J. C., Lovell, P. A., Lai-Cheong, J. E., Graham, R. M., Mellerio, J. E., McGrath, J. A.   +7 more
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Junctional epidermolysis bullosa: a case report

International Journal of Paediatric Dentistry, 2005
Summary.Epidermolysis bullosa (EB) is a group of genetically determined disorders characterized by blistering of the skin and mucosae. There are three major forms – simple, junctional and dystrophic – and each has several varieties. The present case report describes a male child with junctional EB.
A, Momeni, K, Pieper
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Junctional Epidermolysis bullosa with Urethral Stricture

Dermatologica, 2009
We present a case of junctional epidermolysis bullosa (EB) associated with urethral tract involvement. He was a 27-year-old man who had symblepharon of the right eye, hoarseness and urethral stricture in addition to generalized blister formation.
M, Ichiki, M, Kasada, H, Hachisuka, Y, Sasai   +3 more
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Phenytoin and Junctional Epidermolysis Bullosa

Archives of Dermatology, 1985
To the Editor.— We read with great interest the article by Rogers et al 1 on the use of phenytoin in the treatment of junctional epidermolysis bullosa (JEB). We are in complete agreement with the authors regarding the value of this drug in treating JEB and recessive dystrophic epidermolysis bullosa (RDEB), but we have certain reservations about the ...
M, Armoni, M, Schlesinger, P A, Vardy, A, Metzker   +3 more
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PRENATAL DIAGNOSIS OF JUNCTIONAL EPIDERMOLYSIS BULLOSA

Lancet, The, 1989
R A J Eady, O M V Schofield, K H Nicolaides   +2 more
exaly   +2 more sources