Imaging Keratitis-Icthyosis-Deafness (KID) syndrome with FDG-PET (F18-fluorodeoxiglucose-Positron Emission Tomography)
| Autor: | Randy Hawkins, Eric Cho, Daniela Arcienega, Carina Mari Aparici |
|---|---|
| Rok vydání: | 2010 |
| Předmět: |
Pathology
medicine.medical_specialty Nuclear Medicine/Molecular Imaging medicine.diagnostic_test business.industry education Rare entity medicine.disease humanities Vascularizing keratitis Keratitis carbohydrates (lipids) Dysplasia Positron emission tomography otorhinolaryngologic diseases medicine Radiology Nuclear Medicine and imaging Radiology business human activities Kid syndrome |
| Zdroj: | Journal of Radiology Case Reports. 4 |
| ISSN: | 1943-0922 |
| DOI: | 10.3941/jrcr.v4i7.381 |
| Popis: | 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. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|