Familial amyloidotic polyneuropathy --Portuguese type-- clinical and neurophysiologic course.

Authors

  • I Conceição Serviço de Neurologia, Centro de Estudos Egas Moniz, Hospital de Santa Maria, Lisboa.
  • M Carvalho
  • M Alves
  • M L Luís

DOI:

https://doi.org/10.20344/amp.3051

Abstract

Sixteen (16) patients with Familial Amyloidotic Polyneuropathy-Portuguese Type (FAP) were evaluated longitudinally, using the EMG and Clinical protocols with the aim of establishing the clinical and neurophysiological evolution rate of FAP. We conclude that spontaneous evolution of FAP patients shows a linear progression. Clinical and neurophysiological evolution times are parallel, with the EMG scores being higher than Clinical ones. We propose that Clinical and EMG scores should be used in the evaluation of future therapeutic trials, namely immunodepuration and liver transplantation.

Downloads

Download data is not yet available.

How to Cite

1.
Conceição I, Carvalho M, Alves M, Luís ML. Familial amyloidotic polyneuropathy --Portuguese type-- clinical and neurophysiologic course. Acta Med Port [Internet]. 1993 Jan. 30 [cited 2024 Mar. 28];6(1):15-7. Available from: https://actamedicaportuguesa.com/revista/index.php/amp/article/view/3051

Issue

Section

Arquivo Histórico