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90 Possible Causes for Autistic Features, Mild Nystagmus

  • Optic Atrophy-Intellectual Disability Syndrome

    Obsessive-compulsive behavior and autistic features have been reported in a single individual. Hypotonia may be present.[disorders.eyes.arizona.edu] Many infants with this condition, especially those who have the more severe forms of the disorder, also have mild to severe neurological issues.[disabilitybenefitscenter.org] Carrier females had mild intellectual disability and mild dysmorphic features.[egl-eurofins.com]

  • Isolated optic nerve hypoplasia

    The identification and measurement of autistic features in children with optic nerve hypoplasia, "isolated" hypopituitarism and varying combinations of septo-optic Dysplasia[etheses.bham.ac.uk] Most infants with ONH have involuntary, rapid eye movements (nystagmus) and/or mild to severe visual impairment of one or both eyes.[rarediseases.org] Vision impairment from ONH ranges from mild to severe and may affect one or both eyes.[aapos.org]

  • Epilepsy

    , or dysmorphic features in males.[ncbi.nlm.nih.gov] (15%), nystagmus (40%), sedation (15%), fine tremor (28%) Ravi Sudhir 1995 No adverse events reported N/A N/A Figures and Tables - Table 5.[doi.org] Autism Spectrum Disorder and/or autistic features were noted in six females from three of our families. Obsessive features were also prominent in our families.[brain.oxfordjournals.org]

  • Dilated Cardiomyopathy Type 2B

    […] with or without Cardiac Defects 2 Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia 3 Mental Retardation With Language Impairment And Autistic Features[preventiongenetics.com] […] dystrophy Optic nerve hypoplasia, bilateral Ornithine carbamoyltransferase deficiency Osler hemorrhagic telangiectasia syndrome Osteoarthritis of hip Osteoarthritis with mild[pentacorelab.hu] features 613670 605515 Autosomal dominant FOXP2 7q31.1 Speech-language disorder-1 602081 605317 Autosomal dominant FOXP3 Xp11.23 Immunodysregulation, polyendocrinopathy,[mnglabs.com]

  • Autosomal Dominant Mental Retardation 21

    Patients also manifest autistic features and other behavioral abnormalities. DYSEIDD transmission pattern is consistent with autosomal recessive inheritance.[genecards.org] […] dominant type 6) 19p13.2 with CAG repeats in α 1A -voltage–dependent calcium channel gene (exonic); CACNA1A protein, P/Q type calcium channel subunit Ataxia and dysarthria, nystagmus[accesspharmacy.mhmedical.com] Investigation of autistic features among individuals with mild to moderate Cornelia de Lange Syndrome. Am J Med Genet. 2012;158:1841-1847.[rarediseases.org]

  • Warburg Micro Syndrome 3

    Some children will eventually display autistic features. Although less common, seizures can also occur.[rarediseases.org] Such mild phenotypic variability of WARBM1 is not well understood.[ojrd.biomedcentral.com] Surprisingly, some WARBM1-associated neuro-ophthalmological anomalies were absent in our patients, such as ptosis and nystagmus, delayed myelination, cerebral atrophy, and[ojrd.biomedcentral.com]

  • Primary Optic Atrophy

    Obsessive-compulsive behavior and autistic features have been reported in a single individual. Hypotonia may be present.[disorders.eyes.arizona.edu] The only symptom is slowly progressive bilateral vision loss, usually mild until late in life.[merckmanuals.com] Many infants with this condition, especially those who have the more severe forms of the disorder, also have mild to severe neurological issues.[disabilitybenefitscenter.org]

  • Adenylosuccinate Lyase Deficiency

    As a result, patients may have variable combinations of psychomotor retardation and/or regression, seizures, autistic features and cerebellar vermis hypoplasia.[ncbi.nlm.nih.gov] - Neurologic Central Nervous System - Psychomotor delay, - Mental retardation Mild - Hypotonia - - Gait ataxia First two years of life - Inability to walk - - Poor eye contact[ijponline.biomedcentral.com] The symptoms are variable and include psychomotor retardation, autistic features, hypotonia, and seizures.[ncbi.nlm.nih.gov]

  • Ataxia

    […] are most closely associated with the autistic features, and whether these pathologic findings cause the behavioral aberrations.[doi.org] ‘The most common adverse effects are somnolence, dizziness, ataxia, fatigue and nystagmus.’[en.oxforddictionaries.com] Episodic ataxia Episodic ataxia is a rare and unusual type of hereditary ataxia where someone experiences episodes of ataxia, but the rest of the time they have no or only mild[nhs.uk]

  • Hyperalaninemia

    : Developmental delay, hypotonia, extrapyramidal movements, seizures, autistic behavior Treatment: Creatine supplementation Cystinosis See Table Lysosomal Transport Defects[merckmanuals.com] Hyperactivity Feeding difficulties Ptosis Micrognathia Flexion contracture Intellectual disability, mild Failure to thrive High pitched voice Cognitive impairment Delayed[mendelian.co] […] transporter of proline, hydroxyproline, and glycine Not determined Biochemical profile: Elevated urinary proline, hydroxyproline, and glycine but normal plasma levels Clinical features[merckmanuals.com]

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