Results 1 -
10
of
34
for
Childhood Onset dystonia
- ... Mutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism-dystonia. Nat Commun. 2016 May 27;7:11601. doi: ...
- ... Mutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism-dystonia. Nat Commun. 2016 May 27;7:11601. doi: ...
- ... s intelligence. The signs and symptoms of early-onset isolated dystonia tend to occur in mid-childhood or adolescence. Abnormal muscle spasms in an arm ...
- ... Dystonia 6 can appear at any age from childhood through adulthood; the average age of onset is 18.The signs and symptoms of dystonia 6 vary among affected individuals. The disorder usually ...
- ... to the specific features of alternating hemiplegia of childhood. More About This Health Condition Multiple variants in the ATP1A3 gene have been found to cause a rare movement disorder called rapid-onset dystonia parkinsonism. This disorder is characterized by the abrupt ...
- ... ear (sensorineural hearing loss), which begins in early childhood. The hearing ... while others have difficulty coordinating movements (ataxia). The ...
- Paroxysmal Dystonia & Dyskinesias (Dystonia Medical Research Foundation)Movement Disorders/Specifics ... Movement Disorders ... Dystonia Medical Research Foundation ... Paroxysmal Dystonia & Dyskinesias are episodic movement disorders in which ...
- Fahr's Syndrome (National Institute of Neurological Disorders and Stroke)Genetic Brain Disorders/Specifics ... Genetic Brain Disorders ... National Institute of Neurological Disorders and Stroke ... From the National Institutes of Health ... Fahr's ...
- ... this form of the disorder, including muscle tensing (dystonia), uncontrolled ... ISOD survive into childhood or adolescence; because of the rarity of this ...
- ... of normal. Those whose movement problems appear in childhood or later tend to have somewhat higher levels of ... Genetic Testing Registry: Classic ...