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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