From Wikipedia, the free encyclopedia
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