Low Voice, Spasmodic Dysphonia, and Hand Dystonia as Clinical Clues for KMT2B-Associated Early-Onset Dystonia

Neuropediatrics. 2018 Oct;49(5):356. doi: 10.1055/s-0038-1661343. Epub 2018 Jun 18.

Authors

Annette Hackenberg¹, Matias Wagner², Jan Pahnke³, Petra Zeitler⁴, Eugen Boltshauser¹

Affiliations

¹ Department of Pediatric Neurology, University Children's Hospital, Zürich, Switzerland.
² Institute of Human Genetics, Technical University of Munich, Munich, Germany.
³ ENT Practice, Rigi Health Center, Küssnacht, Switzerland.
⁴ Pediatric Practice, Rigi Health Center, Küssnacht, Switzerland.

PMID: 29913530
DOI: 10.1055/s-0038-1661343

No abstract available

Publication types

Case Reports

MeSH terms

Child
Dysphonia / genetics*
Dystonic Disorders / genetics*
Histone-Lysine N-Methyltransferase / genetics*
Humans
Male

Substances

Histone-Lysine N-Methyltransferase
KMT2B protein, human