MANGANO S.

Mowat-Wilson syndrome is a genetic disorder associated with a variable phenotype including peculiar facial features associated with intellectual disability, epilepsy, language impairment, and multiple congenital anomalies caused by heterozygous mutation of the ZEB2 gene. The ZEB2 protein is a complex transcription factor that encompasses...

Benign myoclonic epilepsy in infancy (BMEI) is a rare syndrome included among idiopathic generalized epilepsies (IGE) and syndromes with age-related onset. Recently, it has been shown that a few patients with BMEI later had other epilepsy types mainly IGE but never childhood absence epilepsy (CAE). We report a patient who at 11 months of age...

No description

This chapter illustrates some of the main findings of the research that was conducted by the WP6 (Genoa Unit) within the European 7th F.P.—Project "MEDCHANGe" in Marrakesh between the Spring of 2014 and the Winter of 2015. We assumed that Morocco was an interesting fieldwork to investigate the relationships between tourism, culture, subjective...

No description

No description