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Camisa disease
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]

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.