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DYT16: the original cases.

Sarah Camargos¹, Andrew J Lees, Andrew Singleton

¹Movement Disorders Clinic, Hospital das Clínicas, Departamento de Clínica, Médica, Faculdade de Medicina da Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.

Journal of Neurology, Neurosurgery, and Psychiatry

|July 31, 2012

Summary

This summary is machine-generated.

DYT16, a rare genetic disorder, presents as generalized dystonia or dystonia-parkinsonism. This condition, caused by PRKRA gene mutations, is unresponsive to common treatments.

Area of Science:

Genetics
Neurology
Molecular Biology

Background:

DYT16 is an autosomal recessive neurological disorder.
It is associated with mutations in the PRKRA gene.

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The condition manifests as dystonia-parkinsonism.