Literature DB >> 12210373

Clinical variant of familial amyloid polyneuropathy.

Dianna Quan1, Jeffrey A Cohen.   

Abstract

Hereditary amyloidosis with early and prominent peripheral nerve involvement is often designated familial amyloid polyneuropathy (FAP). The abnormality usually lies in the transthyretin (TTR) gene. We describe a patient with a tyr77 TTR gene mutation who presented with sensorimotor polyneuropathy but no other systemic symptoms of amyloidosis. This is one of a few documented cases of the tyr77 mutation in North America. The clinical and electrophysiologic features of this unusual cause of sensorimotor polyneuropathy are discussed. Copyright 2002 Wiley Periodicals, Inc.

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Year:  2002        PMID: 12210373     DOI: 10.1002/mus.10208

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  4 in total

1.  Patterns of neuropathy and autonomic failure in patients with amyloidosis.

Authors:  Annabel K Wang; Robert D Fealey; Tonette L Gehrking; Phillip A Low
Journal:  Mayo Clin Proc       Date:  2008-11       Impact factor: 7.616

2.  Microheterogeneity of transthyretin in serum and ascitic fluid of ovarian cancer patients.

Authors:  Beate Gericke; Jens Raila; Jalid Sehouli; Sophie Haebel; Dominique Könsgen; Alexander Mustea; Florian J Schweigert
Journal:  BMC Cancer       Date:  2005-10-17       Impact factor: 4.430

3.  Myelination, axonal loss and Schwann cell characteristics in axonal polyneuropathy compared to controls.

Authors:  Eva Placheta-Györi; Lea Maria Brandstetter; Jakob Zemann-Schälss; Sonja Wolf; Christine Radtke
Journal:  PLoS One       Date:  2021-11-04       Impact factor: 3.240

4.  Characterization of the microheterogeneity of transthyretin in plasma and urine using SELDI-TOF-MS immunoassay.

Authors:  Florian J Schweigert; Kerstin Wirth; Jens Raila
Journal:  Proteome Sci       Date:  2004-09-01       Impact factor: 2.480

  4 in total

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