| Literature DB >> 22470741 |
Carina Mari Aparici1, Daniela Arcienega, Eric Cho, Randy Hawkins.
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.Entities:
Keywords: FDG; Icthyosis; KID syndrome; Keratitis; PET; deafness
Year: 2010 PMID: 22470741 PMCID: PMC3303363 DOI: 10.3941/jrcr.v4i7.381
Source DB: PubMed Journal: J Radiol Case Rep ISSN: 1943-0922