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2,290 Possible Causes for Cerebellar Hypoplasia, Dysmetria, Non-Communicating Isolated Syringomyelia

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

  • Arnold-Chiari Malformation Type 1

    Cerebellum compression will cause ataxia, dysmetria and incoordination, The CSF block will cause symptoms of upper neck pain and headaches with coughing or sneezing.[neckandback.com] hypoplasia without displacement of the cerebellum through the foramen magnum probably a variation of cerebellar hypoplasia Chiari V malformation absent cerebellum herniation[radiopaedia.org] Compression of cerebellum may result in ataxia, dysmetria, nystagmus, and dysequilibrium.[physio-pedia.com]

  • Dysequilibrium Syndrome

    From Wikipedia, the free encyclopedia Jump to navigation Jump to search VLDLR-associated cerebellar hypoplasia Other names Dysequilibrium syndrome, DES ; Nonprogressive cerebellar[en.wikipedia.org] cerebellar ataxia associated with cerebellar hypoplasia.[ncbi.nlm.nih.gov] An autosomal recessive syndrome of nonprogressive cerebellar ataxia and mental retardation is associated with inferior cerebellar hypoplasia and mild cerebral gyral simplification[ncbi.nlm.nih.gov]

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

    They may also have difficulty with movements that involve judging distance or scale ( dysmetria ).[en.wikipedia.org] SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 2; SCAR2, Cerebellar Granular Cell Hypoplasia and Mental Retardation, Congenital, Cpd 3 Annotation Sufficiency: ?[monarchinitiative.org] Gait ataxia, dysarthria, dysmetria, nystagmus, muscle wasting and dystonia are seen in the late stages of the disease.[patient.info]

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

    Language development deficit Late-onset speech development Poor language development Speech and language delay Speech and language difficulties Speech delay [ more ] 0000750 Dysmetria[rarediseases.info.nih.gov] Localized cerebellar hypoplasia. Fetal coronal T2 image ( A ) shows a left-sided cerebellar hematoma ( arrow ).[ajnr.org] In addition to these eye movement abnormalities, patients had developmental delays and ataxia, nystagmus, dysarthria, tremor, dysmetria, and seizures The epilepsies.[epilepsygenetics.net]

    Missing: Non-Communicating Isolated Syringomyelia
  • Autosomal Recessive Spastic Ataxia with Leukoencephalopathy

    Other variable features include dysarthria, dysmetria, mild cognitive impairment, urinary urgency and dystonic positioning.[uniprot.org] Related phenotypes are hyperreflexia and cerebellar hypoplasia[malacards.org] Dysmetria MedGen UID: 68583 • Concept ID: C0234162 • Finding A type of ataxia characterized by the inability to carry out movements with the correct range and motion across[ncbi.nlm.nih.gov]

    Missing: Non-Communicating Isolated Syringomyelia
  • Autosomal Recessive Spinocerebellar Ataxia 18

    Phenotypic manifestations commonly consist of cerebellar dysarthria, gait ataxia, and dysmetria.[karger.com] Localized cerebellar hypoplasia. Fetal coronal T2 image ( A ) shows a left-sided cerebellar hematoma ( arrow ).[ajnr.org] Cardinal features - Cerebellar pathology – Stance and gait – Poor regulation and coordination of skilled movements (Dysmetria and dysdiadokinesia) – Eye movement disturbances[slideshare.net]

    Missing: Non-Communicating Isolated Syringomyelia
  • Cerebellar Stroke

    Andreason suggests the presence of cognitive dysmetria due to cerebellar involvement in schizophrenia which is analogous to motor dysmetria so far described in cerebellar[ijpm.info] Inherited metabolic disorders - eg, Leigh's disease and the mitochondrial disorders Congenital: Developmental anomalies - eg, cerebellar hypoplasia, Dandy-Walker syndrome[patient.info] Dysmetria and ataxia were most resistant to rehabilitation.[cerebellumandataxias.biomedcentral.com]

    Missing: Non-Communicating Isolated Syringomyelia
  • Autosomal Recessive Spinocerebellar Ataxia 8

    They may also have difficulty with movements that involve judging distance or scale (dysmetria).[ghr.nlm.nih.gov] QT SYNDROME 4 CARDIAC ARRHYTHMIA, ANKYRIN-B-RELATED Ataxin-1 (N76/3, N76/8) SPINOCEREBELLAR ATAXIA 1 CASK (K56A/50) MENTAL RETARDATION AND MICROCEPHALY WITH PONTINE AND CEREBELLAR[neuromab.ucdavis.edu] […] begin in adulthood 0003581 Autosomal recessive inheritance 0000007 Cerebellar atrophy Degeneration of cerebellum 0001272 Dysarthria Difficulty articulating speech 0001260 Dysmetria[rarediseases.info.nih.gov]

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

    Cerebellar exam findings, such as ataxia, vertigo, and dysmetria, are associated with other forms of cerebellar insult besides inherited disorders.[clinicaladvisor.com] This is the first example of the genetic mapping of a pure congenital cerebellar hypoplasia syndrome.[ncbi.nlm.nih.gov] Localized cerebellar hypoplasia. Fetal coronal T2 image ( A ) shows a left-sided cerebellar hematoma ( arrow ).[ajnr.org]

    Missing: Non-Communicating Isolated Syringomyelia
  • Myelocerebellar Disorder

    Nystagmus, dysmetria, increased deep tendon reflexes, and clonus are common. Gait impairment and other neurologic abnormalities are slowly progressive.[gepedia.com] […] severe variant of DC, with the additional manifestations of cerebellar hypoplasia, microcephaly, and psychomotor retardation.4, 5, 6 Most patients with DC have very short[hiv-proteases.com] […] progressive cerebellar ataxia or balance impairment with cerebellar atrophy and periventricular white matter T2 hyperintensities in brain MRI, horizontal and vertical nystagmus, dysmetria[rarediseases.info.nih.gov]

    Missing: Non-Communicating Isolated Syringomyelia

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