Volume 35, Issue 2 pp. 163-166

Granulation tissue in the eyelid margin and conjunctiva in junctional epidermolysis bullosa with features of laryngo–onycho–cutaneous syndrome

Edwin C Figueira MS(Ophth)

Edwin C Figueira MS(Ophth)

Ophthalmology Department, Prince of Wales Hospital,

Search for more papers by this author
Anne Crotty FRCPA

Anne Crotty FRCPA

Hunter New England Health Pathology,

Search for more papers by this author
Christopher J Challinor FRANZCO

Christopher J Challinor FRANZCO

Department of Ophthalmology, John Hunter Hospital, Newcastle, New South Wales, Australia

Search for more papers by this author
Minas T Coroneo FRANZCO

Minas T Coroneo FRANZCO

Ophthalmology Department, Prince of Wales Hospital,

University of New South Wales,

Search for more papers by this author
Dedee F Murrell FAAD

Corresponding Author

Dedee F Murrell FAAD

University of New South Wales,

Department of Dermatology, St George Hospital, and

Multidisciplinary EB Clinic, Sydney Children's Hospital, Sydney, and

Associate Professor Dedee F Murrell, Head, Department of Dermatology, St George Hospital, University of New South Wales, Kogarah, Sydney, NSW 2217, Australia. Email: [email protected]Search for more papers by this author
First published: 14 March 2007
Citations: 15

Abstract

Eye and adnexal involvement in epidermolysis bullosa can range from symptoms of mild irritation resulting from conjunctival involvement to severe cicatrization of the ocular surface and adnexa. We describe a unique case of granulation tissue in the eyelid margin and conjunctiva in a patient with junctional epidermolysis bullosa. The eyelid granulation tissue resembled granulomas that seen in laryngo–onycho–cutaneous syndrome, which is caused by a mutation in an isoform of the LAMA3 gene, LAMA3a. On investigation, our patient had a combination of a unique mutation in LAMA3 and the mutation I17N in LAMA3a, providing further evidence that laryngo–onycho–cutaneous syndrome is a variant of junctional EB.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.