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.
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Authors | Carina Mari Aparici, Daniela Arcienega, Eric Cho, Randy Hawkins |
Journal | Journal of radiology case reports
(J Radiol Case Rep)
Vol. 4
Issue 7
Pg. 6-11
( 2010)
ISSN: 1943-0922 [Print] United States |
PMID | 22470741
(Publication Type: Journal Article)
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