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17 Possible Causes for Cerebrospinal Fluid Protein Increased, Distal Renal Tubular Acidosis, Progressive Polyneuropathy

  • Multiple Myeloma

    […] to multiple myeloma The initial presentation occasionally is a polyneuropathy when it is part of a POEMS syndrome (mostly the sclerotic form).[] However, some patients may have cerebrospinal fluid (CSF) abnormalities; specifically, increased protein and decreased soluble β-amyloid or ApoE.[] Trial-ineligibility was determined by presence of at least one of the common exclusion criteria: heart/renal failure, liver/renal diseases, polyneuropathy, HIV positivity.[]

  • Amyloidosis

    Tafamidis is a TTR stabilizer that is orally administered and, by interfering with amyloid fibril formation and deposition, is capable of slowing progression of TTR polyneuropathy[] Specifically, hereditary ATTR amyloidosis with polyneuropathy (hATTR-PN), also referred to as familial amyloidotic polyneuropathy (FAP) is an inherited, progressive, life-threatening[] Oral tafamidis therapy has inhibited the progression of neurological and cardiovascular symptoms this far.[]

  • Systemic Amyloidosis

    Hou X, Aguilar MI, Small DH (2007) Transthyretin and familial amyloidotic polyneuropathy. Recent progress in understanding the molecular mechanism of neurodegeneration.[] Patients usually present with familial amyloid polyneuropathy, with progressive peripheral and autonomic neuropathy; involvement of the heart or kidneys is variable.[] Progressive cardiac amyloidosis following liver transplantation for familial amyloid polyneuropathy: implications for amyloid fibrillogenesis.[]

  • Systemic Lupus Erythematosus

    fluid (CSF), protein may be elevated and there may be an increase in the number of mononuclear cells.[] progressive course of acute demyelinating polyneuropathy have been reported.[] Interferon-inducible protein 10/CXCL10 is increased in the cerebrospinal fluid of patients with central nervous system lupus. Arthritis Rheum. 2004 ; 50(11): 3731 – 2.[]

  • Familial Progressive Polyneuropathy

    Abstract The purpose of this study was to evaluate the clinical and pathological features in patients with progressive-type familial amyloidotic polyneuropathy (FAP) using[] tubular acidosis with deafness ATP6V1B1 Renal tubular acidosis, distal, autosomal recessive ATP6V0A4 Renal tubular acidosis, proximal, with ocular abnormalities SLC4A4 Renale[] Diagnostic pitfalls include inadequate attention of neurologists to autonomic symptoms, decreased nerve conduction velocity and increased protein content in the cerebrospinal[]

  • Hypertrophic Interstitial Neuropathy

    356.4 specified type NEC 356.8 in diseases classified elsewhere - see Polyneuropathy, in leg NEC 355.8 lower extremity NEC 355.8 upper extremity NEC 354.9 progressive hypertrophic[] […] syndrome Distal renal tubular acidosis Distal renal tubular acidosis with anemia Distal spinal muscular atrophy Distal spinal muscular atrophy type 2 Distal spinal muscular[] […] in the total protein in cerebrospinal fluid.[]

  • CANOMAD Syndrome

    Progression is rare. Late-onset HSMN should be differentiated from chronic idiopathic axonal polyneuropathy in which sensory features and progression are characteristic.[] renal tubular acidosis - See SLC4A1-associated distal renal tubular acidosis Classic Ehlers-Danlos syndrome - See Classical Ehlers-Danlos syndrome Classic ependymoma - See[] Cerebrospinal fluid analysis Investigate CIDP and leptomeningeal lymphomatous infiltration. Elevated protein level is common in PPN.[]

  • MELAS Syndrome

    […] bilateral sensorineural hearing loss and sensitive distal polyneuropathy with increasing muscle weakness.[] In present article we discuss an unusual case of 28 years female in which primary hypothyroidism is associated with distal renal tubular acidosis without evidence of renal[] Lumbar puncture was performed, revealing slight elevation of protein in the cerebrospinal fluid (CSF) but no increased cell count.[]

  • Leigh's Disease

    Neurological symptoms include cognitive impairment, hypotonia, ataxia, tremor, polyneuropathy, hyporeflexia, seizures, as well as generalized weakness.[] Neurology 17:472–482 Google Scholar Salcedo JR (1981) Personal communication Google Scholar Salcedo JR, Hodjati H, Hirschman GH, Chan JCM (1976) Distal renal tubular acidosis[] : A high lactic acid and pyruvic acid (acids found in the mitochondria) concentration in cerebrospinal fluid (CSF) and blood An increase in protein concentration in CSF Muscle[]

  • Atypical Krabbe Disease due to Saposin A Deficiency

    , hearing loss, ataxia, retinitis pigmentosa, and cataract ACO2 Infantile cerebellar-retinal degeneration, Optic atrophy ADCK3 Coenzyme Q10 deficiency, Progressive cerebellar[] Deafness 3 Renal Tubular Acidosis, Distal, Autosomal Dominant 3 Renal Tubular Acidosis, Distal, Autosomal Recessive 3 Renal Tubular Acidosis, Distal, With Hemolytic Anemia[] Oculofaríngea Duchenne Fragilidad del Cromosoma X Neuropatía Tomaculosa Prader Willi Síndrome de Angelman PANELES: ABCB7 Anemia, sideroblastic, and spinocerebellar ataxia ABHD12 Polyneuropathy[]

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