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27 Possible Causes for Hyperlipidemia Type 5, Progressive Polyneuropathy, Thrombocytopenia

  • Chronic Alcoholism

    Leukopenia and Thrombocytopenia due to direct bone marrow effect, but also from cirrhosis/splenomegaly.[] In chronic alcoholism, macrocytosis, thrombocytopenia, prolonged PT, elevated GGT, hyperuricaemia or hypertriglyceridaemia may be found.[] […] continuous Alcoholism, chronic, episodic Cerebral degeneration due to alcoholism Continuous chronic alcoholism Episodic chronic alcoholism Postpartum alcohol dependence Thrombocytopenia[]

  • Multiple Myeloma

    KEYWORDS: Multiple myeloma; autoimmun hemolytic anemia; evan s syndrome; thrombocytopenia[] […] to multiple myeloma The initial presentation occasionally is a polyneuropathy when it is part of a POEMS syndrome (mostly the sclerotic form).[] Moreover, there was much more largely decreased incidence of grade 3 and higher thrombocytopenia and BIPN in bortezomib SC administration than IV route.[]

  • Waldenstrom Macroglobulinemia

    , leads to an improvement of concurrent thrombocytopenia.[] Neuropathy is typically slowly progressive, distal, symmetrical, and sensorimotor.[] His severe thrombocytopenia and attendant bleeding manifestations were attributed to an immune thrombocytopenia.[]

  • Diabetes Mellitus

    Metagenomic analysis of fever, thrombocytopenia and leukopenia syndrome (FTLS) in Henan Province, China: discovery of a new bunyavirus.[] Evaluation and management of thrombocytopenia and suspected heparin-induced thrombocytopenia in hospitalized patients: the Complications After Thrombocytopenia Caused by Heparin[] In the CATCH (Complications After Thrombocytopenia Caused by Heparin) registry, 530, 531 thrombocytopenia was common among those who received heparin for 96 hours (36.4%)[]

  • Propionic Acidemia

    Severe thrombocytopenia is the hallmark of the metabolic crisis.[] […] demyelination, which results in progressive neurologic dysfunction, includ-ing pyramidal signs, polyneuropathy, bulbar symptoms, ataxia, or even psychiatric symptoms in adult[] […] due to hepatic triacylglycerol lipase deficiency Hyperlipoproteinemia type 1 Hyperlipoproteinemia type 3 Hyperlipoproteinemia type 5 Hyperlysinemia Hypermethioninemia due[]

  • Neuropathy

    Sensory BIPN represented the most common grade 3/4 toxicity, followed by leukopenia, neutropenia, dizziness, and thrombocytopenia.[] Most types of polyneuropathy progress fairly slowly, over months or years, but rapidly progressive polyneuropathy also occurs.[] Obesity and hyperlipidemia are risk factors for early diabetic neuropathy. J Diabet Complicat. 2013;27(5):436–42.[]

  • Autosomal Recessive Spastic Paraplegia Type 14

    Your recognised location is United States (US) Thrombocytopenia This article is freely available only to users in the UK.[] Finally, disease progression seemed slow as all patients were able to walk after disease durations up to 15 years.[] hyperlipidemia with adipose tissue dysfunction Combined familial hyperlipidemia with dysfunctional LDL clearance Combined familial hyperlipidemia with dysfunctional VLDL[]

  • Neuronal Ceroid Lipofuscinosis

    […] chromosome 8 dentinogenesis imperfecta EXT1 gene RAD21 gene SHANK3 gene SYNGAP1 gene trichorhinophalangeal syndrome type II TRPS1 gene June 27, 2017 Behçet disease immune thrombocytopenia[] Visual failure was noticed at 6 years of age, but thereafter disease progression was atypical.[] […] due to hepatic triglyceride lipase deficiency Hyperlipidemia type 3 Hyperlipoproteinemia type 1 Hyperlipoproteinemia type 3 Hyperlipoproteinemia type 4 Hyperlipoproteinemia[]

  • Hypergonadotropic Hypogonadism-Cataract Syndrome

    Progressive bone marrow failure with pancytopenia typically presents in the first decade, often initially with thrombocytopenia or leukopenia.[] Two sisters with mental retardation, cataract, ataxia, progressive hearing loss, and polyneuropathy. J Med Genet 1991 ; 28 : 884 –5.[] type 3 Alpha-thalassemia x-linked intellectual disability syndrome Goblet cell carcinoid Myotonic dystrophy type 2 Familial partial lipodystrophy 5-alpha reductase deficiency[]

  • Chudley-Rozdilsky Syndrome

    Syndrome thiamine-responsive megaloblastic anemia syndrome Thomas Jewett Raines Syndrome Thomas Syndrome Thompson Baraitser Syndrome Thoracic Dysplasia-Hydrocephalus Syndrome Thrombocytopenia[] peripheral neuropathy with arthrogryposis multiplex - See Neuropathy, congenital, with arthrogryposis multiplex Congenital nonprogressive spinocerebellar ataxia - See Spinocerebellar[] type 3 / Hyperlipoproteinemia type 5 / Hyperlysinemia / Hypermethioninemia due to S-adenosylhomocysteine hydrolase deficiency / Hypermobile Ehlers-Danlos syndrome / Hyperostosis[]

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