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{{mergefrom|Childhood linear IgA disease|date=August 2013}} |
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{{mergefrom|Childhood linear IgA disease|date=August 2013}} |
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'''Linear IgA bullous dermatosis''' (also known as "Linear IgA dermatosis") is frequently associated with medication exposure, especially ], with men and women being equally affected.<ref name="Andrews">James, William; Berger, Timothy; Elston, Dirk (2005). ''Andrews' Diseases of the Skin: Clinical Dermatology''. (10th ed.). Saunders. ISBN 0-7216-2921-0.</ref>{{rp|135}} Linear IgA dermatosis is a rare immune-mediated blistering skin disease that may be divided into two types, ] and ].<ref name="Fitz2">Freedberg, et al. (2003). ''Fitzpatrick's Dermatology in General Medicine''. (6th ed.). McGraw-Hill. ISBN 0-07-138076-0.</ref>{{rp|587}} |
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'''Linear IgA bullous dermatosis''' (also known as "Linear IgA dermatosis") is frequently associated with medication exposure, especially ], with men and women being equally affected.<ref name="Andrews">James, William; Berger, Timothy; Elston, Dirk (2005). ''Andrews' Diseases of the Skin: Clinical Dermatology''. (10th ed.). Saunders. ISBN 0-7216-2921-0.</ref>{{rp|135}} Linear IgA dermatosis is a rare immune-mediated blistering skin disease that may be divided into two types:<ref name="Fitz2">Freedberg, et al. (2003). ''Fitzpatrick's Dermatology in General Medicine''. (6th ed.). McGraw-Hill. ISBN 0-07-138076-0.</ref>{{rp|587}} |
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* ''Adult linear IgA disease'' is an acquired, autoimmune blistering disease that may present with a clinical pattern of vesicles indistinguishable from dermatitis herpetiformis, or with vesicles and bullae in a bullous pemphigoid-like appearance. <ref name="Andrews"/> |
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* ''Childhood linear IgA disease'' (also known as "Chronic bullous disease of childhood") is an acquired, self-limited bullous disease that may begin by the time the patient is age 2 to 3 and usually remits by age 13. <ref name="Andrews"/> |
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==See also== |
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==See also== |
