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3,449 Possible Causes for Cerebellar Ataxia, Cerebellar Hypoplasia, Non-Communicating Isolated Syringomyelia

Did you mean: Cerebellar Ataxia, Cerebellar Hypoplasia, Non-Communicating, Isolated Syringomyelia

  • Arnold-Chiari Malformation Type 1

    ataxia 0002073 Scoliosis Abnormal curving of the spine 0002650 Sensory impairment 0003474 Stiff neck Neck stiffness 0025258 Syringomyelia Fluid-filled cyst in spinal cord[] hypoplasia without displacement of the cerebellum through the foramen magnum probably a variation of cerebellar hypoplasia Chiari V malformation absent cerebellum herniation[] Truncal and appendicular ataxia, & cerebellar dysfunction, is the second most common sign (in 30–40%). 5.[]

  • Dysequilibrium Syndrome

    Dysequilibrium syndrome is a genetically heterogeneous condition that combines autosomal recessive, nonprogressive cerebellar ataxia with mental retardation.[] From Wikipedia, the free encyclopedia Jump to navigation Jump to search VLDLR-associated cerebellar hypoplasia Other names Dysequilibrium syndrome, DES ; Nonprogressive cerebellar[] cerebellar ataxia associated with cerebellar hypoplasia.[]

    Missing: Non-Communicating Isolated Syringomyelia
  • Dandy-Walker Syndrome

    Marinesco-Sjögren syndrome (MSS) is a rare autosomal recessive disorder, which is characterized by congenital cataracts, cerebellar ataxia, progressive muscle weakness, and[] hypoplasia, hydrocephalus, and posterior fossa cyst formation.[] Neurological examination was unremarkable without cerebellar ataxia or psychomotor retardation .the patient was submitted to CT scan and magnetic resonance imaging (MRI) of[]

    Missing: Non-Communicating Isolated Syringomyelia
  • Congenital Non-Progressive Ataxia

    Since that time the syndrome of cerebellar ataxia, oligophrenia, and congenital cataracts has become known as the Marinesco-Sjogren syndrome.[] Clinical evaluation showed bilateral superior coloboma, foveal hypoplasia, and inferior cerebellar hypoplasia.[] In many cases, neuroimaging studies (CT scan, MRI) show cerebellar hypoplasia or atrophy, especially of the vermis, with occasional white matter changes, and diffuse atrophy[]

    Missing: Non-Communicating Isolated Syringomyelia
  • Aprosencephaly and Cerebellar Dysgenesis

    […] tremor/ataxia syndrome (FXTAS)- – mild to moderate cerebral & cerebellar atrophy – Increases T2 signal in deep white matter of cerebellar hemisphere & middle cerebellar peduncles[] This article is about human cerebellar hypoplasia. For cerebellar hypoplasia in other animals, see cerebellar hypoplasia (non-human).[] ataxia, and mental retardation, see Gillespie syndrome aniridia-cerebellar ataxia-intellectual disability, see Gillespie syndrome aniridia-cerebellar ataxia-mental deficiency[]

    Missing: Non-Communicating Isolated Syringomyelia
  • Myelocerebellar Disorder

    Ataxia-pancytopenia (AP) syndrome is seen as a cerebellar ataxia, variable hematologic cytopenias, and predisposition to marrow failing and myeloid leukemia, connected with[] hypoplasia Lissencephaly with cerebellar hypoplasia type A Lissencephaly with cerebellar hypoplasia type B Lissencephaly with cerebellar hypoplasia type C Lissencephaly with[] […] disorders in cerebellar ataxia were not treatable.[]

    Missing: Non-Communicating Isolated Syringomyelia
  • X-Linked Spinocerebellar Ataxia Type 5

    Both cases featured congenital hypotonia, delayed motor development, and cerebellar ataxia.[] This is the first example of the genetic mapping of a pure congenital cerebellar hypoplasia syndrome.[] Localized cerebellar hypoplasia. Fetal coronal T2 image ( A ) shows a left-sided cerebellar hematoma ( arrow ).[]

    Missing: Non-Communicating Isolated Syringomyelia
  • Cerebellotrigeminal Dermal Dysplasia

    Ancillary Article Information Format Available Full text: PDF Request Permissions Keywords symmetrical scalp alopecia; craniosynostosis; cerebellar ataxia; rhombencephalosynapsis[] Neuroimaging of patients with GLHS shows rhombencephalosynapsis is universally present, with ventriculomegaly/hydrocephalus and cerebellar hypoplasia being common.[] Poretti A, Limperopoulos C, Roulet-Perez E et al (2010) Outcome of severe unilateral cerebellar hypoplasia.[]

    Missing: Non-Communicating Isolated Syringomyelia
  • Adult-Onset Autosomal Recessive Cerebellar Ataxia

    Tags: acute onset cerebellar ataxia , autosomal recessive cerebellar ataxia , cerebellar ataxia , cerebellar dysfunction , Friedreich's ataxia , neurodegenerative diseases[] SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 2; SCAR2, Cerebellar Granular Cell Hypoplasia and Mental Retardation, Congenital, Cpd 3 Annotation Sufficiency: ?[] Localized cerebellar hypoplasia. Fetal coronal T2 image ( A ) shows a left-sided cerebellar hematoma ( arrow ).[]

    Missing: Non-Communicating Isolated Syringomyelia
  • Infantile-Onset Autosomal Recessive Nonprogressive Cerebellar Ataxia

    Applicable To Early-onset cerebellar ataxia with essential tremor Early-onset cerebellar ataxia with myoclonus [Hunt's ataxia] Early-onset cerebellar ataxia with retained[] Localized cerebellar hypoplasia. Fetal coronal T2 image ( A ) shows a left-sided cerebellar hematoma ( arrow ).[] The Blueprint Genetics ataxia panel covers classical genes associated with cerebellar ataxia, spinocerebellar ataxia and episodic ataxia.[]

    Missing: Non-Communicating Isolated Syringomyelia

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