Hailey-Hailey disease (Conditions)
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Conditions (26):
Darier's Disease, Genetic and Rare Conditions, Ehlers-Danlos syndrome, and 23 others
Darier's Disease, Genetic and Rare Conditions, Ehlers-Danlos syndrome, Marfan syndrome, Angelman syndrome, Friedreich's Ataxia, Menkes Kinky Hair Syndrome, Huntington's disease, Sjogren's Syndrome, Behcet's Syndrome, Inflammatory Linear Verrucous Epidermal Nevus, Skin and Hair, Epidermal Nevus, Fragile X Syndrome, Ichthyosis Vulgaris, Skin Abnormalities, Retinitis Pigmentosa, Tuberous Sclerosis, Cri-du-Chat Syndrome, Addison's Disease, Elephantiasis, Williams Syndrome, Keratosis Follicularis Squamosa, Achalasia, CREST Syndrome, Lichen Planus [hide]
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Groups (37):
Hailey-Hailey disease, Darier's Disease, Beckers Nevus, and 34 others
Hailey-Hailey disease, Darier's Disease, Beckers Nevus, Lichen Sclerosis, Lichen Planus, Hidradenitis Suppurativa, Sweet Syndrome, Granuloma Annulare, Alopecia Areata, Achalasia, Rare 'Orphan' Disorders, Hirschsprung's Disease, PANDAS Syndrome, Agenesis of Corpus Callosum, Dercum's Disease, Trimethylaminuria, Addison's Disease, Anencephaly, Blepharophimosis, Dandy Walker Syndrome, Fragile X Syndrome, Pachygyria, Ledderhose Disease, Aarskog Syndrome, Legg-Calve-Perthes Disease, Microphthalmia, Cri-du-Chat Syndrome, Behcet's Syndrome, Cleidocranial Dysplasia, Fructose Intolerance, 1p36 Deletion Syndrome, Kartagener Syndrome, Empty Sella Syndrome, Cushing's Syndrome, Menkes Kinky Hair Syndrome, Eczema, Androgen Insensitivity Syndrome [hide]
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Symptoms (26):
Von Willebrand disease, Scleroderma, Blepharophimosis, and 23 others
Von Willebrand disease, Scleroderma, Blepharophimosis, Sweet Syndrome, Club Foot, pyoderma gangrenosum, Granuloma Annulare, Castleman's Disease, Alopecia Areata, Tetralogy of Fallot, Raynaud's Disease and Phenomenon, red skin rash, Angioedema, Mole, Port-Wine Stain, keratinization, Bulla, Wernicke-Korsakoff Syndrome, Hypopigmentation, Sclerodactyly, Skin Findings, Organic brain syndrome, Kallmann Syndrome, Fear of cancer of skin, Infected finger/toe/paronychia, Cryoglobulinemia [hide]
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Treatments (10):
achondroplasia, Relaxation of scar or web contracture of skin, hydroquinone 40 MG/ML Topical Cream, and 7 others
achondroplasia, Relaxation of scar or web contracture of skin, hydroquinone 40 MG/ML Topical Cream, Dermabrasion, HYDROQUINONE 4 %, dioxybenzone 30 MG/ML / ETHYL DIHYDROXYPROPYL PABA 50 MG/ML / hydroquinone 40 MG/ML Topical Cream, Other OR therapeutic procedures on skin and breast, hydroquinone 40 MG/ML / padimate-O 30 MG/ML Topical Cream, HYDROQUINONE 2 %, Electrolysis and other epilation of skin [hide]
About Hailey-Hailey disease
Familial benign pemphigus originally was described by the Hailey brothers in 1939, and is commonly called Hailey-Hailey disease.
It is characterized by outbreaks of rashes and blisters in the skin, usually in the folds of the skins, but also often over large areas of the body. The painful blisters break... more 
Familial benign pemphigus originally was described by the Hailey brothers in 1939, and is commonly called Hailey-Hailey disease.
It is characterized by outbreaks of rashes and blisters in the skin, usually in the folds of the skins, but also often over large areas of the body. The painful blisters break and sometimes become infected and raw, with new blisters forming over raw skin in a sometimes seemingly unending cycles of outbreaks.
The cause of the disease is a defect in the calcium pump ATP2C1 gene which is located on chromosome 3. This causes the cells of the skin to not adhere together properly, causing the blisters and rashes. There is no cure.
Steroidal cremes have some effect during outbreaks, but do not stop them. Avoiding heat and friction of affected areas and keeping the area clean and dry work about as well.
Some have found relief in laser surgery that apparently burns off the top layer of the dermis, allowing healthy non-affected skin to regrow in its place, but this method of treatment is new to the disease and lacks the tests of time.
Unfortunately, there is not much that really helps when the outbreaks come, except to suffer through them, "suffer" being the key word here, since the outbreaks are often extremely painful.
It is characterized by outbreaks of rashes and blisters in the skin, usually in the folds of the skins, but also often over large areas of the body. The painful blisters break and sometimes become infected and raw, with new blisters forming over raw skin in a sometimes seemingly unending cycles of outbreaks.
The cause of the disease is a defect in the calcium pump ATP2C1 gene which is located on chromosome 3. This causes the cells of the skin to not adhere together properly, causing the blisters and rashes. There is no cure.
Steroidal cremes have some effect during outbreaks, but do not stop them. Avoiding heat and friction of affected areas and keeping the area clean and dry work about as well.
Some have found relief in laser surgery that apparently burns off the top layer of the dermis, allowing healthy non-affected skin to regrow in its place, but this method of treatment is new to the disease and lacks the tests of time.
Unfortunately, there is not much that really helps when the outbreaks come, except to suffer through them, "suffer" being the key word here, since the outbreaks are often extremely painful.
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