Literature DB >> 7231878

Congenital obstruction of the lacrimal passages in five consecutive generations.

F Moro, S Li Volti, S Tomarchio, L Pavone, M Martorina, F Mollica.   

Abstract

Congenital epiphora due to absence or imperfection of lacrimal puncta and/or canaliculi was present in 21 members from five consecutive generations of a Sicilian family. The anomaly was transmitted as an autosomal-dominant characteristic with apparently complete penetrance and highly variable expressivity.

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Year:  1980        PMID: 7231878     DOI: 10.1159/000309040

Source DB:  PubMed          Journal:  Ophthalmologica        ISSN: 0030-3755            Impact factor:   3.250


  1 in total

1.  Preliminary report on screening IGSF3 gene mutation in families with congenital absence of lacrimal puncta and canaliculi.

Authors:  Fei Wang; Hai Tao; Cui Han; Fang Bai; Peng Wang; Xi-Bin Zhou; Li-Hua Wang; Chuan Liu
Journal:  Int J Ophthalmol       Date:  2020-09-18       Impact factor: 1.779

  1 in total

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