Epidermolysis bullosa acquisita

Classification	D ICD-10: L12.3; ICD-9-CM: 694.8; MeSH: D016107; DiseasesDB: 4338;
External resources	eMedicine: article/1063083; Orphanet: 46487;

Epidermolysis bullosa acquisita
Other names	Acquired epidermolysis bullosa[1]
Specialty	Dermatology

Epidermolysis bullosa acquisita is a chronic subepidermal blistering disease associated with autoimmunity to type VII collagen[2] within anchoring fibril structures that are located at the dermoepidermal junction.[3]^:609

References

RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Acquired epidermolysis bullosa". www.orpha.net. Retrieved 19 April 2019.
Helen Chapel; Mansel Haeney; Siraj Misbah (2006). Essentials of clinical immunology. Wiley-Blackwell. pp. 207–. ISBN 978-1-4051-2761-5. Retrieved 25 June 2010.
Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). McGraw-Hill. ISBN 978-0-07-138076-8.

External links

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[1] RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Acquired epidermolysis bullosa". www.orpha.net. Retrieved 19 April 2019.

[ChapelHaeney2006-2] Helen Chapel; Mansel Haeney; Siraj Misbah (2006). Essentials of clinical immunology. Wiley-Blackwell. pp. 207–. ISBN 978-1-4051-2761-5. Retrieved 25 June 2010.

[Fitz2-3] Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). McGraw-Hill. ISBN 978-0-07-138076-8.

Classification	D ICD-10: L12.3 ICD-9-CM: 694.8 MeSH: D016107 DiseasesDB: 4338
External resources	eMedicine: article/1063083 Orphanet: 46487

Epidermolysis bullosa acquisita

See also

References

External links