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29 Possible Causes for Ataxia, Hyperlipidemia Type 5, Progressive Polyneuropathy

  • Chronic Alcoholism

    There was a progressive development of parkinsonism, cerebellar ataxia, and mental deterioration by the time he was 32.[ncbi.nlm.nih.gov] Others develop for non-hereditary reasons, such as alcoholic cerebellar ataxia. What Is Cerebellar Ataxia? Cerebellar ataxia is a symptom, not a distinct disorder.[promises.com] […] neuropathy) and central nervous sytem : Cognitive dysfunction, Cerebellar degeneration, Wernicke’s encephalopathy (acute reversible syndrome of psychosis, ophthalmoplegia, and ataxia[errolozdalga.com]

  • Waldenstrom Macroglobulinemia

    Features related to hyperviscosity syndrome include bleeding in the nose or mouth, blurring or loss of vision, headache, dizziness, and difficulty coordinating movements (ataxia[ghr.nlm.nih.gov] Neuropathy is typically slowly progressive, distal, symmetrical, and sensorimotor.[emedicine.medscape.com] Related characteristics hyperviscosity syndrome include nasal and mouth bleeding, blurred vision or loss of vision, headache, dizziness and ataxia.[ivami.com]

  • Diabetes Mellitus

    Friedreich ataxia (FRDA) is a multisystem autosomal recessive disease with progressive clinical course involving the neuromuscular and endocrine system.[ncbi.nlm.nih.gov] Genetic: Wolfram's syndrome (which is also referred to as DIDMOAD: diabetes insipidus, diabetes mellitus, optic atrophy and deafness). [ 2 ] Friedreich's ataxia.[patient.info] Friedreich ataxia 6. Huntington’s chorea 7. Lawrence-Moon-Biedel syndrome 8. Myotonic dystrophy 9. Porphyria 10. Prader-Willi syndrome IV.[omicsonline.org]

  • Multiple Myeloma

    […] to multiple myeloma The initial presentation occasionally is a polyneuropathy when it is part of a POEMS syndrome (mostly the sclerotic form).[radiopaedia.org] DADS neuropathy is characterized by predominant distal sensory impairment, ataxia and often tremor, but little or no weakness and has a close association with IgM kappa monoclonal[doi.org] Trial-ineligibility was determined by presence of at least one of the common exclusion criteria: heart/renal failure, liver/renal diseases, polyneuropathy, HIV positivity.[ncbi.nlm.nih.gov]

  • Peripheral Neuropathy

    Most types of polyneuropathy progress fairly slowly, over months or years, but rapidly progressive polyneuropathy also occurs.[en.wikipedia.org] . : Cerebellar ataxia and coeliac disease. Lancet 2004, 362 :1548.[doi.org] Obesity and hyperlipidemia are risk factors for early diabetic neuropathy. J Diabet Complicat. 2013;27(5):436–42.[doi.org]

  • Neuronal Ceroid Lipofuscinosis

    Visual failure was noticed at 6 years of age, but thereafter disease progression was atypical.[ncbi.nlm.nih.gov] We suggest CLN genes should be considered in the molecular analyses of patients presenting with adult-onset autosomal recessive cerebellar ataxia.[ncbi.nlm.nih.gov] […] due to hepatic triglyceride lipase deficiency Hyperlipidemia type 3 Hyperlipoproteinemia type 1 Hyperlipoproteinemia type 3 Hyperlipoproteinemia type 4 Hyperlipoproteinemia[csbg.cnb.csic.es]

  • Neuropathy

    Most types of polyneuropathy progress fairly slowly, over months or years, but rapidly progressive polyneuropathy also occurs.[en.wikipedia.org] Adult onset cerebellar dysfunction with neuropathy is a commonly encountered condition and is usually due to genetic causes such as spinocerebellar ataxia, gluten ataxia,[ncbi.nlm.nih.gov] Obesity and hyperlipidemia are risk factors for early diabetic neuropathy. J Diabet Complicat. 2013;27(5):436–42.[doi.org]

  • Propionic Acidemia

    […] demyelination, which results in progressive neurologic dysfunction, includ-ing pyramidal signs, polyneuropathy, bulbar symptoms, ataxia, or even psychiatric symptoms in adult[docslide.us] Onset may be later in childhood or adolescence with progressive psychomotor / intellectual impairment, hypotonia and ataxia, digestive disorders, and for some epsiodes of[treatable-id.org] […] due to hepatic triacylglycerol lipase deficiency Hyperlipoproteinemia type 1 Hyperlipoproteinemia type 3 Hyperlipoproteinemia type 5 Hyperlysinemia Hypermethioninemia due[se-atlas.de]

  • Autosomal Recessive Spastic Paraplegia Type 18

    CMT2X patients manifest a slowly progressive, peripheral neuropathy affecting the lower limbs and resulting in gait difficulties and distal sensory impairment.[genecards.org] […] by cerebellar atrophy are referred to as autosomal recessive cerebellar ataxias (ARCA).[elsevier.es] hyperlipidemia with adipose tissue dysfunction Combined familial hyperlipidemia with dysfunctional LDL clearance Combined familial hyperlipidemia with dysfunctional VLDL[moldiag.com]

  • Autosomal Recessive Spastic Paraplegia Type 14

    Finally, disease progression seemed slow as all patients were able to walk after disease durations up to 15 years.[academic.oup.com] hyperlipidemia with adipose tissue dysfunction Combined familial hyperlipidemia with dysfunctional LDL clearance Combined familial hyperlipidemia with dysfunctional VLDL[moldiag.com] Symptoms appear in the first decade of life and progress rapidly. The condition is associated with sensorimotor polyneuropathy and occasionally dementia.[elsevier.es]

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