Novel ocular findings in oculodentodigital dysplasia (ODDD): a case report and literature review.

Abstract

BACKGROUND:

Oculodentodigitaldysplasia (ODDD; MIM no. 164200) is a rare hereditary disorder caused by mutations in the gene GJA1.Ocular disorders included microcornea, cornea opacity and glaucoma. However, few studies described fundus findings.

MATERIALS AND METHODS:

Ophthalmic examination included visual acuity measurement, intraocular pressure (IOP) measurements, slit-lamp biomicroscopy, B-scan ultrasonography, Ultrasound biomicroscopy (UBM), spectral-domain optical coherence tomography (SD-OCT), ERG and retcam fluorescein angiogram. In addition, blood samples were taken from this patient for mutation analyze of GJA1.

RESULT:

The ophthalmic features of this patient were microcornea, cornea opacity, glaucoma as expected. Interestingly, the patient had a normal axial length with refractive status of emmetropia, but extremely retinal dysplasia and severe choroid thinning was noted. Flash electroretinogram (ERG) was extinguished in both eyes. This study identified a novel mutation c.91A>T in the GJA1 gene associated with fundus abnormalities. Bioinformatics and structural modeling suggested the mutation to be pathogenic.

CONCLUSION:

Our research expanded not only the mutation spectrum, but also the clinical characteristics of ODDD. To the best of our knowledge, this is the first report on anatomical and functional chorioretinal changes in ODDD patients. These novel ocular features highlight the importance of fundus morphological and functional evaluation in ODDD.

ABBREVIATIONS:

ODDD: oculodentodigital dysplasia; OCT: optical coherence tomography; ERG: electroretinogram; TACT: teller acuity card test; UBM: ultrasound biomicroscopy; MW: molecular weights; AL: axial length; Cx43: connexin 43; RPE: retinal pigment epithelium; RGCs: retinal ganglion cells; FEVR: familial exudative vitreoretinopathy; ROP: retinopathy of prematurity.

• Authors: Zhirong Wang, Limei Sun, Panfeng Wang, Chonglin Chen, Aiyuan Zhang, Weiqing Wang, Xiaoyan Ding
• Journal: Ophthalmic genetics (Ophthalmic Genet) Vol. 40 Issue 1 Pg. 54-59 (02 2019) ISSN: 1744-5094 [Electronic] England
• PMID: 30767687 (Publication Type: Case Reports, Journal Article, Review)

Chemical References

• Connexin 43
• GJA1 protein, human

Topics

• Connexin 43 (genetics)
• Craniofacial Abnormalities (genetics, pathology)
• Eye Abnormalities (genetics, pathology)
• Foot Deformities, Congenital (genetics, pathology)
• Humans
• Infant
• Male
• Microscopy, Acoustic
• Mutation
• Prognosis
• Syndactyly (genetics, pathology)
• Tomography, Optical Coherence
• Tooth Abnormalities (genetics, pathology)