Indian Journal of Ophthalmology

CASE REPORT
Year
: 2018  |  Volume : 66  |  Issue : 2  |  Page : 334--336

Relative anterior microphthalmos in oculodentodigital dysplasia


Orsolya Orosz1, Mariann Fodor1, István Balogh2, Gergely Losonczy3 
1 Department of Ophthalmology, University of Debrecen, Debrecen, Hungary, The Netherlands
2 Department of Laboratory Medicine, Division of Clinical Genetics, University of Debrecen, Debrecen, Hungary, The Netherlands
3 Department of Ophthalmology, University of Debrecen; Department of Ophthalmology, Zuyderland Hospital, Eyescan BV, Sittard, The Netherlands

Correspondence Address:
Dr. Gergely Losonczy
Department of Ophthalmology, University of Debrecen, H-4032, Nagyerdei Krt 98, Debrecen, Hungary
The Netherlands

Here, we report a patient with oculodentodigital dysplasia (ODDD) caused by the c. 413G>A, p.Gly138Asp mutation in the gap junction protein alpha-1 gene. The patient suffered from characteristic dysmorphic features of ODDD. Ophthalmological investigation disclosed microcornea and a shallow anterior chamber, as expected. Surprisingly, the patient had a normal axial length and moderate myopia on both eyes. To the best of our knowledge, this is the first report on ODDD associated with relative anterior microphthalmos and myopia.


How to cite this article:
Orosz O, Fodor M, Balogh I, Losonczy G. Relative anterior microphthalmos in oculodentodigital dysplasia.Indian J Ophthalmol 2018;66:334-336


How to cite this URL:
Orosz O, Fodor M, Balogh I, Losonczy G. Relative anterior microphthalmos in oculodentodigital dysplasia. Indian J Ophthalmol [serial online] 2018 [cited 2024 Mar 29 ];66:334-336
Available from: https://journals.lww.com/ijo/pages/default.aspx/article.asp?issn=0301-4738;year=2018;volume=66;issue=2;spage=334;epage=336;aulast=Orosz;type=0