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89 Possible Causes for Cerebrospinal Fluid Protein Increased, Muscular Atrophy, Progressive Polyneuropathy

  • Chronic Inflammatory Demyelinating Polyneuropathy

    Peroneal muscular atrophy (PMA) and related disorders. I. Clinical manifestations as related to biopsy findings, nerve conduction and electromyography.[] Shortly after HSCT the patient developed progressive polyneuropathy of the lower legs and hypoesthesia. Five months later a severe dementia followed.[] Although cerebrospinal fluid protein levels were often increased in both groups, the elevations were generally mild or moderate in misdiagnosed patients, at an average of[]

  • Guillain-Barré Syndrome

    RESULTS: All six patients had different degrees of muscular atrophy at nadir and in two, respiratory muscles were involved.[] Guillain-Barré syndrome is a rare condition in pregnancy which is characterised by symmetrical progressive ascending polyneuropathy.[] The increase of protein level in cerebrospinal fluid is more marked in recurrent episodes.[]

  • 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.[]

  • Beriberi

    Classically it is characterized by multiple neuritis, muscular atrophy, weakness, cardiovascular changes, and progressive edema. beriberi the name given to thiamin deficiency[] The essential feature is a polyneuropathy. b. The muscles become progressively more wasted and weak, and walking becomes increasingly difficult. c.[]

  • Peripheral Neuropathy

    Muscular atrophy of hand muscles persisted. Large fibers were involved more extensively than small fibers.[] Most types of polyneuropathy progress fairly slowly, over months or years, but rapidly progressive polyneuropathy also occurs.[] Boulis works on novel treatments for several nerve disorders, including Amyotrophic Lateral Sclerosis (ALS, also known as Lou Gehrig's disease) and Spinal Muscular Atrophy[]

  • Hereditary ATTR Amyloidosis

    atrophy (JASMITT study): a multicentre, randomised, double-blind, placebo-controlled trial.[] Rapid progression of familial amyloidotic polyneuropathy: a multinational natural history study. Neurology . 2015;85(8):675-682. Hanna M.[] Specifically, hereditary ATTR amyloidosis with polyneuropathy (hATTR-PN), also referred to as familial amyloidotic polyneuropathy (FAP) is an inherited, progressive, life-threatening[]

  • Déjerine-Sottas Disease

    He is currently involved in multiple clinical trials of novel genetic interventions for the treatment of spinal muscular atrophy and Duchenne muscular dystrophy. Dr. H.[] Synonym(s): Dejerine disease, progressive hypertrophic polyneuropathy. Dejerine, Joseph J., Paris neurologist, 1849-1917.[] In contrast to H MSN I and HMSN II, in which muscular atrophy is limited to the leg, both trunk and limb muscles are involved in Dejerine-Sottas disease.[]

  • Polyneuropathy

    Neuronal Peroneal Muscular Atrophy (HMSN II) Autosomal dominant inheritance is also the case with HMSN II.[] Convert to ICD-10-CM : 356.4 converts directly to: 2015/16 ICD-10-CM G60.3 Idiopathic progressive neuropathy Approximate Synonyms Idiopathic progressive neuropathy Polyneuropathy[] Cerebrospinal fluid protein was raised. Sural nerve biopsy demonstrated decreased numbers of myelinated fibres and inflammatory cell infiltrates.[]

  • Caudal Spinal Cord Tumor

    atrophy Symptoms vary but might include pain, numbness, loss of sensation and muscle weakness.[] However, a more aggressive approach is required when a patient has progressive neurologic deficits. 2 View/Print Table TABLE 2 Conditions Making Spinal Pathology Difficult[] A slight increase in the cerebrospinal fluid (CSF, liquor) protein content detected in patients with all types of oncological compressive myelopathy.[]

  • Metachromatic Leukodystrophy

    The child developed progressive degeneration of the central nervous system, refractory bronchopneumonia, and generalized muscular atrophy.[] Our patient has a progressive peripheral neuropathy but has apparently intact CNS function at her present age of 57 years.[] Biffi, “ which led to an increased expression of the protein in stem cells and in the cerebrospinal fluid.[]

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