Transthyretin-related TTR hereditary amyloidosis of the vitreous body: Clinical and molecular characterisation in two Italian families

F. Salvi, G. Salvi, R. Volpe, R. Mencucci, R. Plasmati, R. Michelucci, P. Gobbi, M. Santangelo, I. Ferlini, A. Forabosco, C. A. Tassinari

Research output: Contribution to journalArticlepeer-review

Abstract

Two unrelated Italian families affected by hereditary amyloidosis are described. Molecular genetic characterization demonstrated different mutations of the transthyretin gene. In all patients belonging to the TTR Ala 49 family the vitreous body, the heart and the peripheral nervous system were massively infiltrated by amyloid matter. In the TTR Pro 36 family vitreous opacities were the long-standing isolated manifestations of the disease. Two different patterns of vitreous deposits can be observed in these two families. The authors' data support the hypothesis that different pathological transthyretin proteins may have different affinity for the connective tissue in the vitreous.

Original languageEnglish
Pages (from-to)9-16
Number of pages8
JournalOphthalmic Paediatrics and Genetics
Volume14
Issue number1
Publication statusPublished - 1993

Keywords

  • Hereditary amyloidosis
  • Transthyretin
  • Vitreous opacities

ASJC Scopus subject areas

  • Genetics(clinical)
  • Ophthalmology
  • Pediatrics, Perinatology, and Child Health

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