2 results match your criteria: "University of Pavia and IRCCS 'C. Mondino'[Affiliation]"

WAGR syndrome: is the 'R' always justified?

Clin Dysmorphol

January 2007

Child Neuropsychiatry Unit, Department of Clinical and Biological Sciences, University of Insubria and Ospedale Fondazione Macchi, Varese Department of Paediatric Surgery, University of Pavia and IRCCS Policlinico 'S. Matteo' Department of Child Neurology and Psychiatry, University of Pavia and IRCCS 'C. Mondino', Pavia, Italy.

Although mild-to-moderate intellectual disability is usually considered part of WAGR syndrome (Wilms' tumour (WT), Aniridia, Genital abnormalities, and metal Retardation, due to 11p13 deletion) the neuropsychological profile of the syndrome is little reported in the literature. We report about a 12-year-old boy presenting with WAGR syndrome (WT, right complete aniridia, bilateral cryptorchidism, interstitial deletion involving band 11p13) but with no mental retardation. An in-depth clinical evaluation revealed no behavioural or social problems and the child's neuropsychological profile was found to be within the normal range for all abilities and functions investigated (with the exception of an impulsive cognitive style and some difficulties in academic skills).

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Vestibular evoked myogenic potentials (VEMPs) are myogenic responses induced by stimulation of the saccular macula by intense sound stimuli. The responses are recordable from the sternocleidomastoid (SCM) muscles. We recorded VEMPs from normal subjects (up to three times in each subject) to identify: i) the best recording procedures, ii) the reliability, and iii) the normal limits for both individual point and test-retest evaluation.

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