Literature DB >> 183858

Peripheral nerve fibre changes in asymptomatic children of patients with familial amyloid polyneuropathy.

J Carvalho, A Coimbra, C Andrade.   

Abstract

Sural nerve biopsies of 5 children of patients with familial amyloid polyneuropathy were studied by electronmicroscopy. The subjects were 14-17 years old and were in normal health. Neurological examination was negative. In none of the sural nerve specimens were there any amyloid deposits. In Case 4 no fine structural changes were detected. In the remaining 4 cases, there were frequent deposits of glycogen and clusters of multimembranous bodies in the Schwann-cell crescents of large myelinated fibres which presented infoldings of the myelin sheath, irregular myelin lamellation and a great number of Schmidt-Lanterman incisures. In one nerve fasciculus of Case 5 the myelin sheaths of some large myelinated fibres were extremely thickened; the axoplasm exhibited dilated vesicles and disordered microfilaments. These findings were taken as evidence of the occurrence of nerve fibre lesions at the pre-symptomatic stage of the disease, which seem to precede the appearance of amyloid deposition. The lesions affected primarily the Schwann cell and myelin sheath, and spared the unmyelinated fibres.

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Year:  1976        PMID: 183858     DOI: 10.1093/brain/99.1.1

Source DB:  PubMed          Journal:  Brain        ISSN: 0006-8950            Impact factor:   13.501


  6 in total

Review 1.  Technetium pyrophosphate myocardial uptake and peripheral neuropathy in a rare variant of familial transthyretin (TTR) amyloidosis (Ser23Asn): a case report and literature review.

Authors:  Adam Castaño; Sabahat Bokhari; Thomas H Brannagan; Julia Wynn; Mathew S Maurer
Journal:  Amyloid       Date:  2011-12-08       Impact factor: 7.141

2.  Plasma catecholamines and postural hypotension in familial amyloidotic polyneuropathy of the Portuguese type.

Authors:  J Ducla-Soares; L Breitenfeld; P Póvoa; M Ferreira; M Carvalho; M Alves; M Bicho; M de L Sales-Luis; C Manso; A da Palma-Carlos
Journal:  Clin Auton Res       Date:  1991-12       Impact factor: 4.435

3.  Comparison of amyloid deposition in two lines of transgenic mouse that model familial amyloidotic polyneuropathy, type I.

Authors:  Y Takaoka; F Tashiro; S Yi; S Maeda; K Shimada; K Takahashi; Y Sakaki; K Yamamura
Journal:  Transgenic Res       Date:  1997-07       Impact factor: 2.788

4.  Biochemical marker in familial amyloidotic polyneuropathy, Portuguese type. Family studies on the transthyretin (prealbumin)-methionine-30 variant.

Authors:  M J Saraiva; P P Costa; D S Goodman
Journal:  J Clin Invest       Date:  1985-12       Impact factor: 14.808

5.  Amyloid fibril protein in familial amyloidotic polyneuropathy, Portuguese type. Definition of molecular abnormality in transthyretin (prealbumin).

Authors:  M J Saraiva; S Birken; P P Costa; D S Goodman
Journal:  J Clin Invest       Date:  1984-07       Impact factor: 14.808

6.  Aqueous outflow system in familial amyloidotic polyneuropathy, Portuguese type.

Authors:  A C Silva-Araújo; M A Tavares; J S Cotta; J F Castro-Correia
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1993-03       Impact factor: 3.117

  6 in total

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