Early-onset movement disorder as diagnostic marker in genetic syndromes: Three cases of FOXG1-related syndrome.

In conclusion, we stress the importance of considering genetic syndromes in the differential diagnosis of early-onset movement disorders.
PMID: 29396177 [PubMed - as supplied by publisher]

Source: European Journal of Paediatric Neurology - January 29, 2018 Category: Neurology Authors: Caporali C, Signorini S, De Giorgis V, Pichiecchio A, Zuffardi O, Orcesi S Tags: Eur J Paediatr Neurol Source Type: research