| Literature DB >> 28786747 |
Paolo Rigamonti1, Silvia Squarza2, Marco Politi3, Roberto Sangermani2, Maurizio Cariati2, Carla Uggetti2.
Abstract
We studied a 9-year-old boy, affected with the Parry-Romberg syndrome, during a period of 32 months, by means of clinical evaluations and neuroradiological magnetic resonance imaging. Over this time we observed a clinical progression of the cutaneous disease without a simultaneous progression of the neurological alterations. Conventional and advanced magnetic resonance imaging techniques showed white matter alterations which proved to be stable during the follow-up.Entities:
Keywords: Parry–Romberg syndrome; follow-up; fractional anisotropy; paediatric; spectroscopy
Mesh:
Year: 2017 PMID: 28786747 PMCID: PMC5602328 DOI: 10.1177/1971400916689577
Source DB: PubMed Journal: Neuroradiol J ISSN: 1971-4009