Imaging Keratitis-Icthyosis-Deafness (KID) syndrome with FDG-PET (F18-fluorodeoxiglucose-Positron Emission Tomography)
DOI:
https://doi.org/10.3941/jrcr.v4i7.381Keywords:
Keratitis, Icthyosis, deafness, KID syndrome, FDG, PETAbstract
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.Downloads
Published
2010-06-27
Issue
Section
Nuclear Medicine / Molecular Imaging
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