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Article

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

Orphanet journal of rare diseases - 16 Feb 2022

Indelicato Elisabetta, Zech Michael, Amprosi Matthias, Boesch Sylvia

Abstract excerpt

BACKGROUND: The genetic landscape of neurodevelopmental disorders is constantly expanding and children with early-onset neurological phenotypes increasingly receive a genetic diagnosis. Nonetheless, the awareness of the chronic course of these conditions, and consequently their recognition and management in the adult population, is still limited. RESULTS: Herein, we describe four patients with rare...

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Identifiers

PMID: 35172867
DOI: 10.1186/s13023-022-02218-8
PMCID: PMC8848801

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