Add to ORKGHailey-Hailey disease is a rare chronic skin disorder that is inherited in an autosomal dominant manner. The disease is characterized by development of vesicles and bullae typically in the intertriginous areas. On histology, there is widespread intraepidermal acantholysis causing the “dilapidated brick-wall” appearance. Mutations in the ATP2C1 gene, encoding for P-type Ca2+ transport ATPase, is the primary cause of the disease. The disease manifests around puberty and runs a chronic course with remissions and exacerbations. Ultraviolet light exposure, sweating, friction, stress, and cutaneous infections are the known precipitants of the disease. We report a case of a woman with recurrent flare-ups of Hailey-Hailey disease with repeated preg...
Background Hailey-Hailey disease (HHD) is a rare autosomal dominant dermatosis. It causes suprabasil...
Benign familial chronic pemphigus (Hailey-Hailey disease, HHD) is a rare hereditary condition charac...
<p>Identification of three novel and one recurrent mutation in <i>ATP2C1</i> in Lebanese families wi...
Hailey-Hailey disease is a rare chronic skin disorder that is inherited in an autosomal dominant man...
Hailey-Hailey disease is an autosomal dominant skin disorder characterized by suprabasal cell separa...
Hailey-Hailey disease is an autosomal dominant skin disorder characterized by suprabasal cell separa...
Hailey-Hailey disease (HHD) is a rare autosomal dominant skin condition discovered in 1939 by Hailey...
Hailey-Hailey disease (HHD), also called as familial benign chronic pemphigus, is a rare autosomal d...
Hailey-Hailey disease is an autosomal dominant skin disorder characterized by suprabasal cell separa...
Hailey-Hailey disease is an autosomal dominant skin disorder characterized by suprabasal cell separa...
Background: Hailey-Hailey disease (HHD) is an autosomal dominant blistering skin disorder that manif...
Hailey Hailey disease or Familial chronic benign pemphigus is a rare autosomal dominant acantholytic...
Background: Hailey-Hailey disease (HHD) is an autosomal dominant disorder with recurrent pruritic ve...
AbstractBackgroundHailey-Hailey disease (HHD) is an autosomal dominant disorder with recurrent pruri...
International audienceMost of the published reports on Hailey-Hailey disease (HHD) come from Europea...
Background Hailey-Hailey disease (HHD) is a rare autosomal dominant dermatosis. It causes suprabasil...
Benign familial chronic pemphigus (Hailey-Hailey disease, HHD) is a rare hereditary condition charac...
<p>Identification of three novel and one recurrent mutation in <i>ATP2C1</i> in Lebanese families wi...
Hailey-Hailey disease is a rare chronic skin disorder that is inherited in an autosomal dominant man...
Hailey-Hailey disease is an autosomal dominant skin disorder characterized by suprabasal cell separa...
Hailey-Hailey disease is an autosomal dominant skin disorder characterized by suprabasal cell separa...
Hailey-Hailey disease (HHD) is a rare autosomal dominant skin condition discovered in 1939 by Hailey...
Hailey-Hailey disease (HHD), also called as familial benign chronic pemphigus, is a rare autosomal d...
Hailey-Hailey disease is an autosomal dominant skin disorder characterized by suprabasal cell separa...
Hailey-Hailey disease is an autosomal dominant skin disorder characterized by suprabasal cell separa...
Background: Hailey-Hailey disease (HHD) is an autosomal dominant blistering skin disorder that manif...
Hailey Hailey disease or Familial chronic benign pemphigus is a rare autosomal dominant acantholytic...
Background: Hailey-Hailey disease (HHD) is an autosomal dominant disorder with recurrent pruritic ve...
AbstractBackgroundHailey-Hailey disease (HHD) is an autosomal dominant disorder with recurrent pruri...
International audienceMost of the published reports on Hailey-Hailey disease (HHD) come from Europea...
Background Hailey-Hailey disease (HHD) is a rare autosomal dominant dermatosis. It causes suprabasil...
Benign familial chronic pemphigus (Hailey-Hailey disease, HHD) is a rare hereditary condition charac...
<p>Identification of three novel and one recurrent mutation in <i>ATP2C1</i> in Lebanese families wi...