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18 Possible Causes for Hypoalbuminemia, Neuronal Loss and Gliosis in the Inferior Olives

  • Disorder of Fructose Metabolism

    […] test: causes hypoglycemia Definitive diagnosis Aldolase B enzyme assay in a liver biopsy sample DNA testing for genetic defect Abnormal liver function tests : AST and ALT, hypoalbuminemia[amboss.com] There was marked depletion of cerebellar Purkinje cells, with sparing of the granular layer and neuronal loss in the dentate nuclei and inferior olives.[clinicalgate.com] In both cases, there was diffuse white matter gliosis, with focal areas of infarction.[clinicalgate.com]

  • Olivopontocerebellar Atrophy

    Serum biochemical abnormalities of low thyroid binding globulin, hypoalbuminemia, and low cholesterol, suggestive of the carbohydrate-deficient glycoprotein syndrome, were[ncbi.nlm.nih.gov] There is neuronal loss and gliosis in the inferior olives, pons, cerebellum, substantia nigra, locus ceruleus, striatum and the intermediolateral column of the spinal cord[dizziness-and-balance.com] […] in the neonatal period with failure to thrive, bilateral pleural and pericardial effusions, and hepatic insufficiency characterized by elevated liver functions tests and hypoalbuminemia[ncbi.nlm.nih.gov]

  • Autosomal Recessive Spinocerebellar Ataxia 8

    T, Takahashi T, Nagatomo H, Sekijima Y,Kawachi I, Takiyama Y, Nishizawa M, Fukuhara N, Saito K, Sugano S, Tsuji S (2001) Early-onset ataxia with ocular motor apraxia and hypoalbuminemia[link.springer.com] Microscopic examination of these structures reveals neuronal loss, axon and myelin degeneration, and gliosis.[neuropathology-web.org] Abbreviations: SCAR-Spinocerebellar ataxia; AOA-Ataxia oculomotor apraxia; EAOH-Early onset ataxia with oculomotor apraxia and hypoalbuminemia; CoQ10D-Coenzyme Q10 deficiency[centogene.com]

  • Dentatorubral-Pallidoluysian Atrophy

    Eight DRPLA patients showed hypoalbuminemia Publication type, MeSH terms, Substances Publication type Research Support, Non-U.S.[ncbi.nlm.nih.gov] Neuropathological examination showed severe neuronal loss associated with gliosis in the inferior olive and cerebellar Purkinje cell layer.[doi.org] Akihiko Ishiyama, Hirofumi Komaki, Eiji Nakagawa, Masayuki Sasaki, Kimiteru Ito, Yuko Saito, Sayuri Sukigara, Masayuki Ito, Yu-ichi Goto, Shuichi Ito and Kentaro Matsuoka, Hypoalbuminemia[doi.org]

  • Autosomal Recessive Spinocerebellar Ataxia

    […] adracalin aladin AAAS 605378 13666 alanyl-tRNA synthetase AARS 601065 20 anoctamin 10 transmembrane protein 16K ANO10 TMEM16K 613726 25519 aprataxin ataxia 1, early onset with hypoalbuminemia[ukgtn.nhs.uk] Microscopic examination of these structures reveals neuronal loss, axon and myelin degeneration, and gliosis.[neuropathology-web.org] Abbreviations: SCAR-Spinocerebellar ataxia; AOA-Ataxia oculomotor apraxia; EAOH-Early onset ataxia with oculomotor apraxia and hypoalbuminemia; CoQ10D-Coenzyme Q10 deficiency[centogene.com]

  • Cerebellar Ataxia with Peripheral Neuropathy Type 2

    Takiyama, et al.Early-onset ataxia with ocular motor apraxia and hypoalbuminemia: the aprataxin gene mutations. Neurology 2002;59(4): 590-5. Takashima, H., C. F.[rarediseases.org] Microscopic examination of these structures reveals neuronal loss, axon and myelin degeneration, and gliosis.[neuropathology-web.org] Abbreviations: SCAR-Spinocerebellar ataxia; AOA-Ataxia oculomotor apraxia; EAOH-Early onset ataxia with oculomotor apraxia and hypoalbuminemia; CoQ10D-Coenzyme Q10 deficiency[centogene.com]

  • Ataxia

    Laboratory evaluation revealed hypoalbuminemia, hypercholesterolemia with elevated LDL, elevated IgE levels and normal α fetoprotein levels.[ncbi.nlm.nih.gov] Microscopic examination of these structures reveals neuronal loss, axon and myelin degeneration, and gliosis.[neuropathology-web.org] Abbreviations: SCAR-Spinocerebellar ataxia; AOA-Ataxia oculomotor apraxia; EAOH-Early onset ataxia with oculomotor apraxia and hypoalbuminemia; CoQ10D-Coenzyme Q10 deficiency[centogene.com]

  • Adult-Onset Autosomal Recessive Cerebellar Ataxia

    Abbreviations: SCAR-Spinocerebellar ataxia; AOA-Ataxia oculomotor apraxia; EAOH-Early onset ataxia with oculomotor apraxia and hypoalbuminemia; CoQ10D-Coenzyme Q10 deficiency[centogene.com] Microscopic examination of these structures reveals neuronal loss, axon and myelin degeneration, and gliosis.[neuropathology-web.org] […] ophthalmoplegia Motor neuropathy, progressive distal amyotrophy Normal cognition in Portuguese families, decline in cognition noted in Japanese families Laboratory findings Hypoalbuminemia[emedicine.medscape.com]

  • Paraneoplastic Neurologic Syndrome

    […] immunocomplexes in nephrons (and subsequent membranoproliferative glomerulonephritis) is thought to be the underlying mechanism of nephrotic syndrome and, frequently, neoplastic hypoalbuminemia[emedicine.medscape.com] In addition, mild secondary neuronal cell loss with gliosis was noted in the dentate nucleus and inferior olive.[jneuroinflammation.com] Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene. Nat Genet. 2001;29:184–8.[jneuroinflammation.com]

  • Spinocerebellar Ataxia Type 13

    […] ophthalmoplegia Motor neuropathy, progressive distal amyotrophy Normal cognition in Portuguese families, decline in cognition noted in Japanese families Laboratory findings Hypoalbuminemia[emedicine.com] loss and gliosis.[link.springer.com] […] recessive 11q22-q23 ATM gene Product belongs to the P-13 kinase family of proteins involved in DNA damage recognition Ataxia with oculomotor apraxia type 1 (AOA1) FRDA-like hypoalbuminemia[emedicine.com]

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