Create issue ticket

142 Possible Causes for Average Intelligence, Generalized Dystonia

  • Primary Torsion Dystonia

    Fifteen of them presented with the typical DYT1 phenotype (early, limb-onset generalized dystonia without spread to craniocervical muscles), four had limb-onset dystonia with[] Three siblings had childhood onset of limb dystonia, and slow progression to generalized dystonia with predominant cranio-cervical involvement.[] Forty-six of them had segmental dystonia and 59 had focal dystonia, The other 23 patients presented with generalized dystonia, either with craniocervical involvement (13 patients[]

  • Movement Disorder

    Dystonia may affect the entire body (generalized dystonia) or one part of the body (focal dystonia). Functional movement disorder.[] Mass General was one of the first hospitals to perform DBS and today we also use it to treat many different types of Dystonia which include: Genetic dysonia Generalized dystonia[] Dystonia: Dystonias were often interpreted in psychological or psychiatric terms since the original descriptions of generalized dystonia by Barraquer Roviralta (1897), and[]

  • Parkinson's Disease

    Aziz, Twiddler’s syndrome in a patient with a deep brain stimulation device for generalized dystonia, Journal of Clinical Neuroscience, 18, 7, (970), (2011). Craig G.[]

  • Amyotrophic Lateral Sclerosis

    It can be localized to a certain group of muscles or can be generalized (180).[] The precise mechanism is not known, although primary dystonia is suspected to be caused by decreased activity within GABA-ergic circuits including those in the basal ganglia[]

  • Chorea Gravidarum

    […] frontotemporal dementia Generalized Epilepsy and Paroxysmal Dyskinesia gestational diabetes Gilles de la Tourette syndrome herpes gestationis Huntington's disease Huntington's[] Status dystonicus, a condition of generalized, unremitting dystonia, is usually limited to patients with pre-existing dystonia and can be precipitated by infection or medication[] DYSTONIA, CHILDHOOD-ONSET, WITH OPTIC ATROPHY AND BASAL GANGLIA ABNORMALITIES Early Onset Parkinsonism with Mental Retardation ectopic pregnancy Fetal Death Fetal Diseases[]

  • Adult-Onset Cervical Dystonia Type DYT23

    DYT1 dystonia typically presents as early onset, generalized dystonia, starting in the legs.[] It is characterized by below-average intelligence or mental ability.[] Multifocal dystonia affects many different parts of the body. Generalized dystonia affects most of the body, frequently involving the legs and back.[]

  • SHORT Syndrome

    […] feet scoliosis (curved spine, associated with spinal asymmetry & accentuated by a short leg) prominent heels [mUPD7 primarily]* autism [mUPD7 children primarily]* myoclonus dystonia[] […] to above-average intelligence.[] Although these children may also possess signs of low blood sugar or obesity, they display average body proportions and (average intelligence.[]

  • Russell-Silver Syndrome

    […] feet scoliosis (curved spine, associated with spinal asymmetry & accentuated by a short leg) prominent heels [mUPD7 primarily]* autism [mUPD7 children primarily]* myoclonus dystonia[] Characteristics of both Small-for-Gestational-Age Children and Russell-Silver Syndrome Patients: lack of interest in eating fasting hypoglycemia & mild metabolic acidosis generalized[]

  • Rheumatic Chorea

    Short-lasting paroxysmal hypnogenic dyskinesia generally is regarded as a form of mesiofrontal epilepsy.[] Intellectual impairment has been reported in one family in which affected individuals had intelligence quotient scores averaging 10 points lower than unaffected relatives.[] Principles in Treatment of Chorea Movement disorders (particularly chorea, athetosis, and dystonia) are thought to result from basal ganglia pathology.[]

  • Spondyloepimetaphyseal Dysplasia Type Strudwick 

    […] polymicrogyria Early infantile epileptic encephalopathy 25 Duane syndrome type 1 Glycogen storage disease type 12 Rapid-onset dystonia-parkinsonism Limb-girdle muscular dystrophy[] The children were judged to be of average intelligence; earlier, mental retardation was thought to be present and to distinguish their disorder from Strudwick dysplasia.[] […] of large deletions and/or duplications in the GCH1 gene by MLPA Dystonia-12 Sanger sequencing of the ATP1A3 gene EBD inversa Next Generation Sequencing and Sanger Sequencing[]

Further symptoms

Similar symptoms