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Imaging Keratitis-Icthyosis-Deafness (KID) syndrome with FDG-PET (F18-fluorodeoxiglucose-Positron Emission Tomography).

Abstract
Keratitis-Icthyosis-Deafness (KID) syndrome is a rare dysplasia characterized by vascularizing keratitis, congenital sensorineural hearing-loss, and progressive erythrokeratoderma. To our knowledge, this is the first KID syndrome imaged with FDG-PET in the literature. This paper is intended to help familiarize with the FDG abnormalities related to this rare entity.
AuthorsCarina Mari Aparici, Daniela Arcienega, Eric Cho, Randy Hawkins
JournalJournal of radiology case reports (J Radiol Case Rep) Vol. 4 Issue 7 Pg. 6-11 ( 2010) ISSN: 1943-0922 [Print] United States
PMID22470741 (Publication Type: Journal Article)

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