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Table 1 Clinical features of the patients; NA: non-applicable

From: Patients with PWS and related syndromes display differentially methylated regions involved in neurodevelopmental and nutritional trajectory

Group Age category Gender Genotype
PWS1 Infant
(1 Year)
Male Deletion type1
PWS2 Child
(10 year)
Male Deletion type1
PWS3 Adult
(27 years)
Female Deletion type2
PWS4 Adult
(32 years)
Male Deletion type2
PWS5 Infant
(1 year)
Male Uniparental disomy
PWS6 Adult
(32 years)
Female SNORD116 microdeletion
PWS7 Adult
(21 years)
Male MAGEL2 mutation
Control Infant
(1 year)
Male NA
Control Infant
(1 year)
Female NA