polyneuropathy

(redirected from amyloid polyneuropathy)
Also found in: Medical.
Related to amyloid polyneuropathy: amyloidosis
Translations

pol·y·neu·rop·a·thy

n. polineuropatía, enfermedad que afecta varios nervios a la vez.
English-Spanish Medical Dictionary © Farlex 2012

polyneuropathy

n polineuropatía
English-Spanish/Spanish-English Medical Dictionary Copyright © 2006 by The McGraw-Hill Companies, Inc. All rights reserved.
References in periodicals archive ?
Depending on the type of mutation, manifestations can range from cardiac involvement (familial cardiac amyloidosis), peripheral nerve damage (familial amyloid polyneuropathy), and overlapping phenotypes [4].
Adams et al., "Ocular involvement in familial amyloid polyneuropathy," Journal Francais d'Ophtalmologie, vol.
M2 PHARMA-September 1, 2017-Pfizer Publishes Long-Term Data Analysis Showing Tafamidis Delays Progression of Hereditary Transthyretin Amyloid Polyneuropathy
The most common forms of amyloidosis include systemic AL amyloidosis (formerly primary amyloidosis), systemic AA amyloidosis (formerly secondary amyloidosis), systemic wild-type ATTR amyloidosis (formerly age-related or senile systemic amyloidosis), systemic hereditary ATTR amyloidosis (formerly familial amyloid polyneuropathy), and localized AL amyloidosis (Table 1).
Familial amyloid polyneuropathy (FAP) type IV (FINNISH) is a very rare life-threatening disorder and reported only in a few countries.
Global Markets Direct's, 'Familial Amyloid Polyneuropathy (Transthyretin Amyloidosis, Corino de Andrade's Disease) - Pipeline Review, H2 2015', provides an overview of the Familial Amyloid Polyneuropathy (Transthyretin Amyloidosis, Corino de Andrade's Disease)'s therapeutic pipeline.
Familial amyloid polyneuropathy. Lancet Neurol 2011;10:1086-97.
to treat transthyretin amyloid polyneuropathy, a fatal disorder of the nervous system that affects about 8,000 people worldwide, Labaudiniere said.
Late-onset familial amyloid polyneuropathy type I (Transthyretin Met30-associated familial amyloid polyneuropathy) unrelated to endemic focus in Japan.
Usefulness of MALDI/TOF mass spectrometry of immuno-precipitated serum variant transthyretin in the diagnosis of familial amyloid polyneuropathy. Amyloid 1999;6:282-8.