Literature DB >> 12036680

Two brothers with gelatinous drop-like dystrophy at different stages of the disease: role of mutational analysis.

Shigeo Yoshida1, Yuji Kumano, Ayako Yoshida, Shin-ichiro Numa, Nobuyuki Yabe, Toshio Hisatomi, Teruo Nishida, Tatsuro Ishibashi, Takao Matsui.   

Abstract

PURPOSE: A report of two Japanese brothers with gelatinous drop-like corneal dystrophy, one with and one without the typical gelatinous drop-like region.
DESIGN: Interventional case report and observational case report.
METHODS: After penetrating keratoplasty, the corneal button, right eye, of the elder brother, 39 years of age, was stained and examined by microscopy. The M1S1 and BIGH3 genes were examined for mutations using the polymerase chain reaction and direct sequencing. Corneal abnormalities in the younger brother, 37 years of age, were observed.
RESULTS: The elder brother had bilateral gelatinous prominences and band-shaped corneal opacities, whereas the younger brother had only bilateral band-shaped opacities. Histologically, corneal deposits beneath the epithelium stained with Congo red. Molecular genetic analysis revealed that M1S1 was homozygously mutated in both brothers (Q118X).
CONCLUSION: The Q118X mutation of the M1S1 gene can produce either a gelatinous drop-like region or band-shaped opacities.

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Year:  2002        PMID: 12036680     DOI: 10.1016/s0002-9394(02)01407-1

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


  5 in total

1.  Presence of vitronectin in neovascularised cornea of patient with gelatinous drop-like dystrophy.

Authors:  S Yoshida; A Yoshida; T Ishibashi; Y Kumano; T Matsui
Journal:  Br J Ophthalmol       Date:  2003-03       Impact factor: 4.638

2.  Chromosomal sharing in atypical cases of gelatinous drop-like corneal dystrophy.

Authors:  Motokazu Tsujikawa; Naoyuki Maeda; Kaoru Tsujikawa; Yuichi Hori; Tomoyuki Inoue; Kohji Nishida
Journal:  Jpn J Ophthalmol       Date:  2010-11-05       Impact factor: 2.447

3.  Rapid genotyping for most common TGFBI mutations with real-time polymerase chain reaction.

Authors:  Shigeo Yoshida; Yoko Yamaji; Ayako Yoshida; Yoshihiro Noda; Yuji Kumano; Tatsuro Ishibashi
Journal:  Hum Genet       Date:  2005-03-03       Impact factor: 4.132

Review 4.  The IC3D classification of the corneal dystrophies.

Authors:  Jayne S Weiss; H U Møller; Walter Lisch; Shigeru Kinoshita; Anthony J Aldave; Michael W Belin; Tero Kivelä; Massimo Busin; Francis L Munier; Berthold Seitz; John Sutphin; Cecilie Bredrup; Mark J Mannis; Christopher J Rapuano; Gabriel Van Rij; Eung Kweon Kim; Gordon K Klintworth
Journal:  Cornea       Date:  2008-12       Impact factor: 2.651

5.  A novel mutation in gelatinous drop-like corneal dystrophy and functional analysis.

Authors:  Yukiko Nagahara; Motokazu Tsujikawa; Toru Takigawa; Peng Xu; Chifune Kai; Satoshi Kawasaki; Mina Nakatsukasa; Tsutomu Inatomi; Shigeru Kinoshita; Kohji Nishida
Journal:  Hum Genome Var       Date:  2019-07-11
  5 in total

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