Literature DB >> 14700667

Two patients with severe corneal disease in KID syndrome.

Shozo Sonoda1, Eisuke Uchino, Koh-Hei Sonoda, Shinichi Yotsumoto, Eiichi Uchio, Yasushi Isashiki, Taiji Sakamoto.   

Abstract

PURPOSE: To report two independent Japanese patients with keratitis, ichthyosis, and deafness (KID) syndrome and severe corneal disorder.
DESIGN: Observational case reports.
METHODS: Clinical observation of a 5-year-old boy (Patient 1) and a 64-year-old man (Patient 2) with KID syndrome, presenting prominent corneal diseases. Molecular genetic assessment of the GJB2 gene encoding connexin-26 was performed.
RESULTS: Patient 1 had bilateral diffuse superficial punctuate keratopathy with severe corneal neovascularization. He had a missense mutation of the GJB2 gene. Patient 2 had bilateral corneal stromal keratitis and right corneal ulceration with rupture of the Descemet membrane. He did not have any pathologic mutation of the GJB2 gene. The area of palisades of Vogt was diminished and tear production reduced in both patients. Topical eye drops, and corticosteroid or antibiotics, respectively, relieved them effectively.
CONCLUSION: The impaired ocular surface regulating system might be a cause of corneal disease in KID syndrome and it can be treated by eye drops.

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Year:  2004        PMID: 14700667     DOI: 10.1016/s0002-9394(03)00739-6

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


  7 in total

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Authors:  Niloofar Bazazzadegan; Abraham M Sheffield; Masoomeh Sobhani; Kimia Kahrizi; Nicole C Meyer; Guy Van Camp; Nele Hilgert; Seyedeh Sedigheh Abedini; Farkhondeh Habibi; Ahmad Daneshi; Carla Nishimura; Matthew R Avenarius; Mohammad Farhadi; Richard J H Smith; Hossein Najmabadi
Journal:  Am J Med Genet A       Date:  2011-04-11       Impact factor: 2.802

2.  Histopathology and treatment of corneal disease in keratitis, ichthyosis, and deafness (KID) syndrome.

Authors:  A R Djalilian; J Y Kim; H N Saeed; E J Holland; C-C Chan
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3.  Klf4 regulates the expression of Slurp1, which functions as an immunomodulatory peptide in the mouse cornea.

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Journal:  Case Rep Dent       Date:  2013-09-18

5.  Altered CO2 sensitivity of connexin26 mutant hemichannels in vitro.

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Journal:  Physiol Rep       Date:  2016-11

6.  Ocular manifestation of Ichthyosis.

Authors:  Mohammad A Al-Amry
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7.  Visual impairment reversal with oral acitretin therapy in keratitis-ichthyosis-deafness (KID) syndrome.

Authors:  Christopher M Wolfe; Alexander Davis; Tarek S Shaath; George F Cohen
Journal:  JAAD Case Rep       Date:  2017-11-08
  7 in total

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