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1,066 Possible Causes for Autosomal Recessive Cerebellar Ataxia

  • Oculomotor Apraxia

    Abstract Autosomal recessive cerebellar ataxias (ARCAs) are a phenotypically and genetically heterogeneous group of diseases.[ncbi.nlm.nih.gov] Keywords Cerebellar Ataxia Apraxia Oculomotor Apraxia Autosomal Recessive Cerebellar Ataxia Autosomal Recessive Ataxia These keywords were added by machine and not by the[link.springer.com] KEYWORDS: AOA2; Autosomal recessive cerebellar ataxia; DNA repair; Helicase; Senataxin[ncbi.nlm.nih.gov]

  • Adult-Onset Autosomal Recessive Cerebellar Ataxia

    Autosomal Recessive Cerebellar Ataxias. May 1, 2013.[en.wikipedia.org] MalaCards based summary : Autosomal Recessive Cerebellar Ataxia with Late-Onset Spasticity, is also known as autosomal recessive cerebellar ataxia due to gba2 deficiency .[malacards.org] Novel ATM mutation in late-onset autosomal recessive cerebellar ataxia with neuropathy. H. Shimazaki 1, R. Sugaya 1, J. Honda 1, A. Meguro 2, I.[ashg.org]

  • Autosomal Recessive Spinocerebellar Ataxia 8

    Autosomal Recessive Cerebellar Ataxias. May 1, 2013.[en.wikipedia.org] SYNE1-Related Autosomal Recessive Cerebellar Ataxia. 2007 Feb 23 [updated 2011 Oct 13].[ghr.nlm.nih.gov] recessive cerebellar ataxia type 3 (ARCA3).[karger.com]

  • Cerebellar Ataxia

    BACKGROUND: Autosomal recessive cerebellar ataxias (ARCA) are a complex group of neurodegenerative disorders with high clinical and genetic heterogeneity.[ncbi.nlm.nih.gov] Autosomal recessive cerebellar ataxia (ARCA) is a group of neurological disorders characterized by degeneration or abnormal development of the cerebellum and spinal cord.[ncbi.nlm.nih.gov] KEYWORDS: Autosomal Recessive Cerebellar Ataxia type 1; Genetic mutation; Multiple sclerosis; SYNE1; White matter disease[ncbi.nlm.nih.gov]

  • Ataxia Telangiectasia

    Autosomal recessive cerebellar ataxia must be considered in any child or young adult with a progressive disorder of gait or balance or with hypotonia or excessive clumsiness[doi.org] recessive cerebellar ataxia, autosomal recessive cerebellar ataxia due to a DNA repair defect Authority control Q387082 Reasonator Scholia Statistics Subcategories This category[commons.wikimedia.org] Ataxia telangiectasia (A-T) is one of a group of autosomal recessive cerebellar ataxias.[ncbi.nlm.nih.gov]

  • Boucher-Neuhäuser Syndrome

    Abstract Background: Autosomal recessive cerebellar ataxias (ARCA) are a complex group of neurodegenerative disorders with high clinical and genetic heterogeneity.[karger.com] […] of cerebellar ataxia and hypogonadotropic hypogonadism.[genome.jp] Abbreviations Abbreviations ARCA autosomal recessive cerebellar ataxia CMT Charcot–Marie–Tooth disease EST phospholipid esterase domain References The autosomal recessive[academic.oup.com]

  • Autosomal Recessive Spinocerebellar Ataxia

    Autosomal Recessive Cerebellar Ataxias. May 1, 2013.[en.wikipedia.org] Resumen : Autosomal recessive cerebellar ataxias (ARCA) are a heterogeneous group of rare neurological disorders involving both central and peripheral nervous system, and[digital.csic.es] [From OMIM:604985, 2015.10.29] Disease synonyms SCAR14 Spectrin-associated autosomal recessive cerebellar ataxia 1 SPARCA1 spinocerebellar ataxia, autosomal recessive 14;[flybase.org]

  • Autosomal Recessive Spinocerebellar Ataxia 18

    Abstract Objective: To report the clinical findings and the genetic linkage mapping of an autosomal recessive cerebellar ataxia associated to peripheral neuropathy, showing[neurology.org] Abstract Background: Autosomal recessive cerebellar ataxias (ARCA) are a complex group of neurodegenerative disorders with high clinical and genetic heterogeneity.[karger.com] Table 1 Autosomal recessive cerebellar ataxias.[wjgnet.com]

  • Autosomal Recessive Spinocerebellar Ataxia Type 17

    Autosomal Recessive Cerebellar Ataxias. May 1, 2013.[ipfs.io] recessive cerebellar ataxia (ARCA).[spatax.wordpress.com] Table 1 Autosomal recessive cerebellar ataxias.[wjgnet.com]

  • Early-Onset Cerebellar Ataxia

    Abstract Autosomal recessive cerebellar ataxias are a heterogeneous group of neurological disorders.[ncbi.nlm.nih.gov] Francesc Palau and Carmen Espinós, Autosomal recessive cerebellar ataxias, Orphanet Journal of Rare Diseases, 10.1186/1750-1172-1-47, 1, 1, (2006).[doi.org] Along with the algorithm, an overview of the autosomal dominant, autosomal recessive, X‐linked, mitochondrial, symptomatic and idiopathic subtypes of cerebellar ataxia is[doi.org]

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