A case of familial amyloid polyneuropathy homozygous for the transthyretinVal30Met gene with motor-dominant sensorimotor polyneuropathy and unusual sural nerve pathological findings

Citation
A. Yoshioka et al., A case of familial amyloid polyneuropathy homozygous for the transthyretinVal30Met gene with motor-dominant sensorimotor polyneuropathy and unusual sural nerve pathological findings, ARCH NEUROL, 58(11), 2001, pp. 1914-1918
Citations number
21
Language
INGLESE
art.tipo
Article
Categorie Soggetti
Neurology,"Neurosciences & Behavoir
Journal title
ARCHIVES OF NEUROLOGY
ISSN journal
0003-9942 → ACNP
Volume
58
Issue
11
Year of publication
2001
Pages
1914 - 1918
Database
ISI
SICI code
0003-9942(200111)58:11<1914:ACOFAP>2.0.ZU;2-8
Abstract
Objective: To report a case of familial amyloid polyneuropathy homozygous f or the amyloidogenic transthyretin (ATTR) Val30Met gene with motor-dominant sensorimotor polyneuropathy and unusual sural nerve pathological findings. Methods: Mass spectrometry analysis and polymerase chain reaction-restricti ng fragment length polymorphism were performed. A right sural nerve biopsy specimen was obtained for histological investigation. Setting: Academic medical center. Results: A 56-year-old japanese man living in a local town (Nakajima, Japan ) in Ishikawa Prefecture, a nonendemic area of type I familial amyloidotic polyneuropathy, had vitreous amyloidosis, motor-dominant sensorimotor polyn europathy, erectile dysfunction, and urinary incontinence. He had neither o rthostatic hypotension nor indolent diarrhea. Restriction enzyme analysis w ith EcoT22 I of amplified DNA and mass spectrometry analysis revealed homoz ygosity for ATTR Val30Met. Of 8 family members, 5 were evaluated and found to be heterozygous for ATTR Val30Met; a family history found no relative wi th the similar neurologic disorders. The sural nerve biopsy specimen showed focal edema and an amyloid deposit in the subperineural tissue, associated with moderate loss of myelinated and unmyelinated fibers. Conclusions: In addition to the findings characteristic of homozygosity for ATTR Val30Met such as vitreous amyloidosis and relatively less autonomic i nvolvements, this case had the unique findings of motor-dominant sensorimot or polyneuropathy and unusual sural nerve biopsy specimen results.