Literature DB >> 11812437

Transthyretin Ser-44 mutation in a case with vitreous amyloidosis.

Akira Murakami1, Keiko Fujiki, Sachiko Hasegawa, Shu Imamura, Hiroyuki Kawano, Atsushi Kanai, Toshiharu Matsumoto.   

Abstract

PURPOSE: To report a case of vitreous amyloidosis associated with a transthyretin Ser-44 mutation.
METHODS: Interventional case report. A 44-year-old Japanese woman had a 2-month history of visual disturbance in both eyes. The vitreous and conjunctival specimens were subjected to histopathological examination. DNA was isolated from peripheral blood cells of the patient. The transthyretin gene was amplified and directly sequenced.
RESULTS: The vitreous and conjunctiva specimens showed typical light microscopic features of amyloidosis. Direct sequencing of the transthyretin gene revealed a single base-pair substitution, which results in an amino acid substitution at position 44, phenylalanine to serine (transthyretin Ser-44).
CONCLUSION: Transthyretin Ser-44 may cause vitreous amyloidosis.

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Year:  2002        PMID: 11812437     DOI: 10.1016/s0002-9394(01)01323-x

Source DB:  PubMed          Journal:  Am J Ophthalmol        ISSN: 0002-9394            Impact factor:   5.258


  1 in total

1.  Transthyretin Arg-83 mutation in vitreous amyloidosis.

Authors:  Ling-Yan Chen; Lin Lu; Yong-Hao Li; Hui Zhong; Wang Fang; Li Zhang; Weng-Lin Li
Journal:  Int J Ophthalmol       Date:  2011-06-18       Impact factor: 1.779

  1 in total

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