Medical condition
Camisa disease Other names Vohwinkel variant with ichthyosis This condition is inherited in an autosomal dominant manner Specialty Dermatology
Camisa disease is the variant form of Vohwinkel syndrome , characterized by ichthyosis and normal hearing.[ 1] : 507, 513
It is associated with loricrin .[ 2] [ 3]
It was characterized in 1984[ 4] and 1988.[ 5]
See also
References
^ Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine . (6th ed.). McGraw-Hill. ISBN 0-07-138076-0 .
^ Matsumoto K, Muto M, Seki S, et al. (October 2001). "Loricrin keratoderma: a cause of congenital ichthyosiform erythroderma and collodion baby". Br. J. Dermatol . 145 (4): 657–60. doi :10.1046/j.1365-2133.2001.04412.x . PMID 11703298 . [dead link ]
^ Korge BP, Ishida-Yamamoto A, Pünter C, et al. (October 1997). "Loricrin mutation in Vohwinkel's keratoderma is unique to the variant with ichthyosis" . J. Invest. Dermatol . 109 (4): 604–10. doi :10.1111/1523-1747.ep12337534 . PMID 9326398 .
^ Camisa C, Rossana C (October 1984). "Variant of keratoderma hereditaria mutilans (Vohwinkel's syndrome). Treatment with orally administered isotretinoin" . Arch Dermatol . 120 (10): 1323–8. doi :10.1001/archderm.120.10.1323 . PMID 6237617 . [permanent dead link ]
^ Camisa C, Hessel A, Rossana C, Parks A (1988). "Autosomal dominant keratoderma, ichthyosiform dermatosis and elevated serum beta-glucuronidase". Dermatologica . 177 (6): 341–7. doi :10.1159/000248604 . PMID 2976687 .
External links
Classification External resources