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Ocular Immunology and Inflammation Volume 17, 2009 - Issue 5
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Original Article

Subretinal Fibrosis and Uveitis Syndrome in a Patient with Ectodermal Dysplasia

Ryan I. HuffmanDepartment of Ophthalmology and Visual Sciences, Yale University School of Medicine, New Haven, CT, USA
&
John J. HuangDepartment of Ophthalmology and Visual Sciences, Yale University School of Medicine, New Haven, CT, USACorrespondence[email protected]
Pages 348-350 | Received 22 Apr 2008, Accepted 07 Jul 2009, Published online: 15 Oct 2009

REFERENCES

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  • Palestine AG, Nussenblatt RB, Parver LM, Knox DL. Progressive subretinal fibrosis and uveitis. Br J Ophthalmol. 1984;68:667–673.
  • Priolo M, Lagana C. Ectodermal dysplasias a new clinical-genetic classification. J Med Genet. 2001;38:579–585.
  • Hill VA, Nischal KK, Collin Harper JI. An unusual ectodermal dysplasia with unique eye defects. Br J Dermatol. 2005;152:365–367.
  • Rodriguez N, Eliott D, Garcia-Valenzuela E, Baker J. Bilateral panuveitis in a child with hypohidrotic ectodermal dysplasia. Am J Ophthalmol. 2002 Sep;134(3):443–445.
  • Zagórski Z, Biziorek B, Rakowska E, Jedrzejewski D. [Zinsser-Engman-Cole syndrome (dyskeratosis congenita) with severe sicca syndrome, panuveitis and corneal perforation—a case report]. Klin Monatsbl Augenheilkd. 2001 Jun;218(6):455–458.
  • Biedner B. Anhidrotic ectodermal dysplasia with relapsing uveitis. Ann Ophthalmol. 1983 Aug;15(8):749–750.
  • Adan A, Sanmarti R, Bures A, Casaroli-Marano RP. Successful treatment with infliximab in a patient with diffuse subretinal fibrosis syndrome. Am J Ophthalmol. 2007;143(3):533–534.

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