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Results 11 - 20 of 72 for Limb dystonia
  1. Tyrosine hydroxylase deficiency 
    ... hydroxylase deficiency (also called TH-deficient dopa-responsive dystonia), symptoms usually appear during childhood. Affected individuals may ... signs and symptoms may include involuntary muscle contractions (dystonia) that lead to abnormal repetitive movements in the ...
    https://medlineplus.gov/.../tyrosine-hydroxylase-deficiency - Genetics
  2. Partington syndrome 
    ... intellectual disability along with a condition called focal dystonia that particularly affects movement of the hands. Partington ... epilepsy) may also occur in Partington syndrome.Focal dystonia of the hands is a feature that distinguishes ...
    https://medlineplus.gov/genetics/condition/partington-syndrome - Genetics
  3. Dopamine transporter deficiency syndrome 
    ... The condition is also known as infantile parkinsonism-dystonia because the problems with movement (dystonia and parkinsonism, described below) usually start in infancy ...
    https://medlineplus.gov/.../dopamine-transporter-deficiency-syndrome - Genetics
  4. Sepiapterin reductase deficiency 
    ... pattern of involuntary, sustained muscle contractions known as dystonia. Other movement problems can include muscle stiffness (spasticity), ... signs and symptoms of the condition. Dopa-responsive dystonia due to sepiapterin reductase deficiency SPR deficiency Genetic ...
    https://medlineplus.gov/.../sepiapterin-reductase-deficiency - Genetics
  5. Benign essential blepharospasm 
    ... the eyelids. This condition is a type of dystonia, which is a group of movement disorders that ... people with benign essential blepharospasm, the symptoms of dystonia spread beyond the eyes to affect other facial ...
    https://medlineplus.gov/.../condition/benign-essential-blepharospasm - Genetics
  6. Autosomal dominant nocturnal frontal lobe epilepsy 
    Autosomal dominant nocturnal frontal lobe epilepsy (ADNFLE) is an uncommon form of epilepsy that runs in families. This disorder causes seizures that usually occur ...
    https://medlineplus.gov/...-dominant-nocturnal-frontal-lobe-epilepsy - Genetics
  7. Pantothenate kinase-associated neurodegeneration 
    Pantothenate kinase-associated neurodegeneration (formerly called Hallervorden-Spatz syndrome) is a disorder of the nervous system. This condition is characterized ...
    https://medlineplus.gov/...enate-kinase-associated-neurodegeneration - Genetics
  8. Beta-propeller protein-associated neurodegeneration 
    ... dementia). Worsening problems with movement also occur, including dystonia and parkinsonism. Dystonia is a condition characterized by involuntary, sustained muscle ...
    https://medlineplus.gov/...ller-protein-associated-neurodegeneration - Genetics
  9. Familial paroxysmal kinesigenic dyskinesia 
    ... An episode may involve slow, prolonged muscle contractions (dystonia); small, fast, "dance-like" motions (chorea); writhing movements ... affected person has one parent with the condition. Dystonia 10 Episodic kinesigenic dyskinesia Familial paroxysmal dystonia Paroxysmal ...
    https://medlineplus.gov/...amilial-paroxysmal-kinesigenic-dyskinesia - Genetics
  10. GLUT1 deficiency syndrome 
    ... as ataxia or involuntary tensing of various muscles (dystonia); the movement problems may be more pronounced than ... deficiency syndrome. These include paroxysmal choreoathetosis with spasticity (dystonia 9); paroxysmal exercise-induced dyskinesia and epilepsy (dystonia ...
    https://medlineplus.gov/genetics/condition/glut1-deficiency-syndrome - Genetics
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