Untangling neurodevelopmental disorders in the adulthood: a movement disorder is the clue.

Elisabetta IndelicatoMichael ZechMatthias AmprosiSylvia Boesch

Published in: Orphanet journal of rare diseases (2022)

This report expands the current knowledge on four rare neurodevelopmental disorders (SON, ZMYND11, DNMT1 and YY1), which was mainly based on reports from paediatric cases. This case series emphasize the importance of a tight neurological surveillance extending beyond the childhood.

Keyphrases

healthcare
dna methylation
intensive care unit
emergency department
blood brain barrier
depressive symptoms
congenital heart disease
adverse drug
electronic health record