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286
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Movement disorder
- ... have been identified in people with congenital mirror movement disorder, a condition in which intentional movements of one ... in the signs and symptoms of congenital mirror movement disorder. More About This Health Condition MedlinePlus Genetics provides ...
- ... have been identified in people with congenital mirror movement disorder, a condition in which intentional movements of one side of the body are mirrored ...
- ... and is characterized by small head size (microcephaly), movement disorders, breathing problems, and seizures. Many of the MECP2 ... role in the development of intellectual disability and movement and mood disorders in affected individuals. More About This Health Condition ...
- ... Sinha S, Mathuranath PS, Taly AB. Hypersomnolence-hyperkinetic movement disorder in a child with compound heterozygous mutation in ...
- ... this disorder include seizures, weak muscle tone (hypotonia), movement disorders, and behavioral problems.Many GRIN2B gene mutations lead ...
- ... people with Leber hereditary optic neuropathy and a movement disorder called dystonia, which involves involuntary muscle contractions, tremors, and other uncontrolled movements. This variant appears to disrupt the normal assembly ...
- ... cases of adult-onset dystonia. Dystonia is a movement disorder that involves involuntary tensing of the muscles (muscle contractions), tremors, and other uncontrolled movements. The MT-ND1 mutation associated with these rare ...
- ... people with dopamine transporter deficiency syndrome, a rare movement disorder that worsens over time. Its signs and symptoms ... less than 5 percent of normal. Those whose movement problems appear in childhood or later ... Health Condition Variations (polymorphisms) in ...
- ... frequent infections. SPENCDI has several additional features, including movement disorders and intellectual disability, but it is unknown how ...
- ... gene have been found to cause a rare movement disorder called rapid-onset dystonia parkinsonism. This disorder is ... of the ATP1A3 gene variants that cause this disorder change single amino acids in ... the movement abnormalities seen in people with rapid-onset dystonia ...
