Camisa disease explained
Camisa disease |
Synonyms: | Vohwinkel variant with ichthyosis |
Field: | Dermatology |
Camisa disease is the variant form of Vohwinkel syndrome, characterized by ichthyosis and normal hearing.[1]
It is associated with loricrin.[2] [3]
It was characterized in 1984[4] and 1988.[5]
See also
Notes and References
- Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). McGraw-Hill. .
- Matsumoto K, Muto M, Seki S . Loricrin keratoderma: a cause of congenital ichthyosiform erythroderma and collodion baby . Br. J. Dermatol. . 145 . 4 . 657–60 . October 2001 . 11703298 . 10.1046/j.1365-2133.2001.04412.x. etal.
- Korge BP, Ishida-Yamamoto A, Pünter C . Loricrin mutation in Vohwinkel's keratoderma is unique to the variant with ichthyosis . J. Invest. Dermatol. . 109 . 4 . 604–10 . October 1997 . 9326398 . 10.1111/1523-1747.ep12337534. etal. free .
- Camisa C, Rossana C . Variant of keratoderma hereditaria mutilans (Vohwinkel's syndrome). Treatment with orally administered isotretinoin . Arch Dermatol . 120 . 10 . 1323–8 . October 1984 . 6237617 . 10.1001/archderm.120.10.1323 .
- Camisa C, Hessel A, Rossana C, Parks A . Autosomal dominant keratoderma, ichthyosiform dermatosis and elevated serum beta-glucuronidase . Dermatologica . 177 . 6 . 341–7 . 1988 . 2976687 . 10.1159/000248604.