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Results 1 - 10 of 15 for Choreoathetosis
  1. Familial paroxysmal nonkinesigenic dyskinesia 
    ... a situation known as reduced penetrance. Familial paroxysmal choreoathetosis Mount-Reback syndrome Nonkinesigenic choreoathetosis Paroxysmal dystonic choreoathetosis ...
    https://medlineplus.gov/...lial-paroxysmal-nonkinesigenic-dyskinesia - Genetics
  2. Lesch-Nyhan syndrome 
    ... cannot pass X-linked traits to their sons. Choreoathetosis self-mutilation syndrome Complete HPRT deficiency Complete hypoxanthine- ... guanine phosphoribosyltransferase deficiency Hypoxanthine ... mental retardation syndrome Juvenile hyperuricemia syndrome Lesch-Nyhan ...
    https://medlineplus.gov/genetics/condition/lesch-nyhan-syndrome - Genetics
  3. Familial paroxysmal kinesigenic dyskinesia 
    ... the condition is known as infantile convulsions and choreoathetosis (ICCA). In families with ICCA, some individuals develop ... Episodic kinesigenic dyskinesia Familial paroxysmal dystonia Paroxysmal kinesigenic choreoathetosis Paroxysmal ... Genetic Testing Registry: Episodic kinesigenic ...
    https://medlineplus.gov/...amilial-paroxysmal-kinesigenic-dyskinesia - Genetics
  4. Brain-lung-thyroid syndrome 
    ... family. BLT syndrome Brain-thyroid-lung syndrome CAHTP Choreoathetosis, hypothyroidism, and neonatal respiratory distress Chreoathetosis and congenital ...
    https://medlineplus.gov/.../condition/brain-lung-thyroid-syndrome - Genetics
  5. Dentatorubral-pallidoluysian atrophy 
    ... symptoms are ataxia, uncontrollable movements of the limbs (choreoathetosis), psychiatric symptoms such as delusions, and deterioration of ... inheritance). DRPLA Haw River syndrome Myoclonic epilepsy with choreoathetosis Naito-Oyanagi disease NOD Genetic Testing Registry: Dentatorubral- ...
    https://medlineplus.gov/.../dentatorubral-pallidoluysian-atrophy - Genetics
  6. NGLY1-congenital disorder of deglycosylation 
    ... abnormalities, such as uncontrolled movements of the limbs (choreoathetosis), and some develop seizures that are difficult to ... Genetic Testing Registry: Congenital disorder of deglycosylation Alacrimia-choreoathetosis-liver dysfunction syndrome National Organization for Rare Disorders ( ...
    https://medlineplus.gov/...y1-congenital-disorder-of-deglycosylation - Genetics
  7. TUBB4A-related leukodystrophy 
    ... muscle contractions (dystonia), uncontrolled movements of the limbs (choreoathetosis), muscle stiffness (rigidity), and difficulty coordinating movements (ataxia). ...
    https://medlineplus.gov/.../condition/tubb4a-related-leukodystrophy - Genetics
  8. GABA-transaminase deficiency 
    ... disorder have recurrent seizures (epilepsy), uncontrolled limb movements (choreoathetosis), exaggerated reflexes (hyperreflexia), weak muscle tone (hypotonia), and ...
    https://medlineplus.gov/.../condition/gaba-transaminase-deficiency - Genetics
  9. Crigler-Najjar syndrome 
    ... problems, including involuntary writhing movements of the body (choreoathetosis), hearing problems, or intellectual disability.Crigler-Najjar syndrome ...
    https://medlineplus.gov/genetics/condition/crigler-najjar-syndrome - Genetics
  10. GLUT1 deficiency syndrome 
    ... variants of GLUT1 deficiency syndrome. These include paroxysmal choreoathetosis with spasticity (dystonia 9); paroxysmal exercise-induced dyskinesia ...
    https://medlineplus.gov/genetics/condition/glut1-deficiency-syndrome - Genetics
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