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Journal of Neurology, Neurosurgery, and Psychiatry logoLink to Journal of Neurology, Neurosurgery, and Psychiatry
. 1988 Apr;51(4):576–578. doi: 10.1136/jnnp.51.4.576

Familial amyloidotic polyneuropathy without familial occurrence: carrier detection by the radioimmunoassay of variant transthyretin.

M Tanaka 1, S Hirai 1, E Matsubara 1, K Okamoto 1, M Morimatsu 1, M Nakazato 1
PMCID: PMC1032978  PMID: 3379433

Abstract

A 47 year old woman with familial amyloidotic polyneuropathy (FAP) is reported, without familial occurrence of the disease. Her 81 year old mother and 53 year old sister were proved to be asymptomatic carriers for variant transthyretin (TTR) by means of the radioimmunoassay. It is suggested that unknown factor(s) may play a role in preventing or delaying the onset of the disease, producing variations in sex and family incidence. In order to establish the diagnosis of non-hereditary primary amyloidotic polyneuropathy, it must be confirmed that variant TTR is absent in the serum of relatives.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Araki S., Mawatari S., Ohta M., Nakajima A., Kuroiwa Y. Polyneuritic amyloidosis in a Japanese family. Arch Neurol. 1968 Jun;18(6):593–602. doi: 10.1001/archneur.1968.00470360015001. [DOI] [PubMed] [Google Scholar]
  2. Dwulet F. E., Benson M. D. Polymorphism of human plasma thyroxine binding prealbumin. Biochem Biophys Res Commun. 1983 Jul 29;114(2):657–662. doi: 10.1016/0006-291x(83)90831-8. [DOI] [PubMed] [Google Scholar]
  3. Kitamoto T., Tateishi J., Hikita K., Nagara H., Takeshita I. A new method to classify amyloid fibril proteins. Acta Neuropathol. 1985;67(3-4):272–278. doi: 10.1007/BF00687812. [DOI] [PubMed] [Google Scholar]
  4. Kito S., Itoga E., Kamiya K., Kishida T., Yamamura Y. Studies on familial amyloid polyneuropathy in Ogawa Village, Japan. Eur Neurol. 1980;19(3):141–151. doi: 10.1159/000115139. [DOI] [PubMed] [Google Scholar]
  5. Mita S., Maeda S., Ide M., Tsuzuki T., Shimada K., Araki S. Familial amyloidotic polyneuropathy diagnosed by cloned human prealbumin cDNA. Neurology. 1986 Feb;36(2):298–301. doi: 10.1212/wnl.36.2.298. [DOI] [PubMed] [Google Scholar]
  6. Nakazato M., Kangawa K., Minamino N., Tawara S., Matsuo H., Araki S. Radioimmunoassay for detecting abnormal prealbumin in the serum for diagnosis of familial amyloidotic polyneuropathy (Japanese type). Biochem Biophys Res Commun. 1984 Jul 31;122(2):719–725. doi: 10.1016/s0006-291x(84)80093-5. [DOI] [PubMed] [Google Scholar]
  7. Nakazato M., Kurihara T., Matsukura S., Kangawa K., Matsuo H. Diagnostic radioimmunoassay for familial amyloidotic polyneuropathy before clinical onset. J Clin Invest. 1986 May;77(5):1699–1703. doi: 10.1172/JCI112489. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Saraiva M. J., Costa P. P., Goodman D. S. Genetic expression of a transthyretin mutation in typical and late-onset Portuguese families with familial amyloidotic polyneuropathy. Neurology. 1986 Nov;36(11):1413–1417. doi: 10.1212/wnl.36.11.1413. [DOI] [PubMed] [Google Scholar]
  9. Tawara S., Nakazato M., Kangawa K., Matsuo H., Araki S. Identification of amyloid prealbumin variant in familial amyloidotic polyneuropathy (Japanese type). Biochem Biophys Res Commun. 1983 Nov 15;116(3):880–888. doi: 10.1016/s0006-291x(83)80224-1. [DOI] [PubMed] [Google Scholar]

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