Ocular findings in Jansen metaphyseal chondrodysplasia

Author:

Obiezu Fiona1ORCID,Magone De Quadros Costa M Teresa2,Huryn Laryssa A2,Pan Kristen1,Almpani Konstantinia3,Ninan Anisha4,Roszko Kelly L1ORCID,Weinstein Lee S4,Gafni Rachel I1,Ferreira Carlos R5,Lee Janice3,Collins Michael T1,Jha Smita4ORCID

Affiliation:

1. National Institute of Dental and Craniofacial Research, National Institutes of Health Skeletal Disorders & Mineral Homeostasis Section, , Bethesda, MD 20892 , United States

2. National Eye Institute, National Institutes of Health , Bethesda, MD 20892 , United States

3. National Institute of Dental and Craniofacial Research, National Institutes of Health Craniofacial Anomalies and Bone Regeneration Section, , Bethesda, MD 20892 , United States

4. National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health Metabolic Diseases Branch, , Bethesda, MD 20892 , United States

5. National Human Genome Research Institute, National Institutes of Health Skeletal Genomics Unit, , Bethesda, MD 20892 , United States

Abstract

Abstract Jansen metaphyseal chondrodysplasia (JMC) is an ultra-rare disorder caused by germline heterozygous PTHR1 variants resulting in constitutive activation of parathyroid hormone type 1 receptor. A description of ocular manifestations of the disease is lacking. Six patients with JMC underwent a detailed ophthalmic evaluation, spectral-domain optical coherence tomography (OCT), visual field testing, and craniofacial CT scans. Five of 6 patients had good visual acuity. All patients had widely spaced eyes; 5/6 had downslanted palpebral fissures. One patient had proptosis, and another had bilateral ptosis. Two patients had incomplete closure of the eyelids (lagophthalmos), one had a history of progressive right facial nerve palsy with profuse epiphora, while the second had advanced optic nerve atrophy with corresponding retinal nerve fiber layer (RNFL) thinning on OCT and significant bilateral optic canal narrowing on CT scan. Additionally, this patient also had central visual field defects and abnormal color vision. A third patient had normal visual acuity, subtle temporal pallor of the optic nerve head, normal average RNFL, but decreased temporal RNFL and retinal ganglion cell layer analysis (GCA) on OCT. GCA was decreased in 4/6 patients indicating a subclinical optic nerve atrophic process. None of the patients had glaucoma or high myopia. These data represent the first comprehensive report of ophthalmic findings in JMC. Patients with JMC have significant eye findings associated with optic canal narrowing due to extensive skull base dysplastic bone overgrowth that appear to be more prevalent and pronounced with age. Progressive optic neuropathy from optic canal narrowing may be a feature of JMC, and OCT GCA can serve as a useful biomarker for progression in the setting of optic canal narrowing. We suggest that patients with JMC should undergo regular ophthalmic examination including color vision, OCT, visual field testing, orbital, and craniofacial imaging.

Funder

Intramural Research Programs of the National Institute of Diabetes and Digestive and Kidney Diseases

National Eye Institute

Publisher

Oxford University Press (OUP)

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