Generalized atrophic benign epidermolysis bullosa

Michelangelo La Placa; Colombina Vincenzi; Pier A. Fanti; Antonella Tosti

doi:10.1016/0926-9959(96)00054-2

Generalized atrophic benign epidermolysis bullosa

Michelangelo La Placa, Colombina Vincenzi, Pier A. Fanti, Antonella Tosti

Research output: Contribution to journal › Article › peer-review

1 Scopus citations

Abstract

Generalized atrophic benign epidermolysis bullosa (GABEB) is a rare autosomal recessive variant of junctional epidermolysis bullosa. A typical feature in these patients is the cicatricial alopecia resembling male pattern baldness: in this paper we describe a case of GABEB with particular attention to this characteristic.

Original language	English (US)
Pages (from-to)	167-170
Number of pages	4
Journal	Journal of the European Academy of Dermatology and Venereology
Volume	7
Issue number	2
DOIs	https://doi.org/10.1016/0926-9959(96)00054-2
State	Published - 1996
Externally published	Yes

Keywords

Bulge activation hypothesis
Generalized atrophic benign epidermolysis bullosa
Junctional epidermolysis bullosa
Laminin

ASJC Scopus subject areas

Dermatology
Infectious Diseases

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

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10.1016/0926-9959(96)00054-2

Cite this

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title = "Generalized atrophic benign epidermolysis bullosa",

abstract = "Generalized atrophic benign epidermolysis bullosa (GABEB) is a rare autosomal recessive variant of junctional epidermolysis bullosa. A typical feature in these patients is the cicatricial alopecia resembling male pattern baldness: in this paper we describe a case of GABEB with particular attention to this characteristic.",

keywords = "Bulge activation hypothesis, Generalized atrophic benign epidermolysis bullosa, Junctional epidermolysis bullosa, Laminin",

author = "{La Placa}, Michelangelo and Colombina Vincenzi and Fanti, {Pier A.} and Antonella Tosti",

year = "1996",

doi = "10.1016/0926-9959(96)00054-2",

language = "English (US)",

volume = "7",

pages = "167--170",

journal = "Journal of the European Academy of Dermatology and Venereology",

issn = "0926-9959",

publisher = "Wiley-Blackwell",

number = "2",

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TY - JOUR

T1 - Generalized atrophic benign epidermolysis bullosa

AU - La Placa, Michelangelo

AU - Vincenzi, Colombina

AU - Fanti, Pier A.

AU - Tosti, Antonella

PY - 1996

Y1 - 1996

N2 - Generalized atrophic benign epidermolysis bullosa (GABEB) is a rare autosomal recessive variant of junctional epidermolysis bullosa. A typical feature in these patients is the cicatricial alopecia resembling male pattern baldness: in this paper we describe a case of GABEB with particular attention to this characteristic.

AB - Generalized atrophic benign epidermolysis bullosa (GABEB) is a rare autosomal recessive variant of junctional epidermolysis bullosa. A typical feature in these patients is the cicatricial alopecia resembling male pattern baldness: in this paper we describe a case of GABEB with particular attention to this characteristic.

KW - Bulge activation hypothesis

KW - Generalized atrophic benign epidermolysis bullosa

KW - Junctional epidermolysis bullosa

KW - Laminin

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U2 - 10.1016/0926-9959(96)00054-2

DO - 10.1016/0926-9959(96)00054-2

M3 - Article

AN - SCOPUS:0029758740

VL - 7

SP - 167

EP - 170

JO - Journal of the European Academy of Dermatology and Venereology

JF - Journal of the European Academy of Dermatology and Venereology

SN - 0926-9959

IS - 2

ER -

Generalized atrophic benign epidermolysis bullosa

Abstract

Keywords

ASJC Scopus subject areas

UN SDGs

Access to Document

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