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Publikováno v:
Journal of Radiology Case Reports. 4
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec5745e1cf599db80f774a342264b6dd
https://doi.org/10.3941/jrcr.v4i7.381
https://doi.org/10.3941/jrcr.v4i7.381
