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

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...

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Hlavní autoři: Aparici, Carina Mari, Arcienega, Daniela, Cho, Eric, Hawkins, Randy
Médium: Artigo
Jazyk:Inglês
Vydáno: EduRad 2010
Témata:
Nuclear Medicine/Molecular Imaging
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3303363/
https://ncbi.nlm.nih.gov/pubmed/22470741
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3941/jrcr.v4i7.381
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