1. Rod bipolar cell dysfunction in POLG retinopathy
- Author
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Anupreet Tumber, Eoghan Millar, Kit Green Sanderson, Neal Sondheimer, Ajoy Vincent, and Regan Klatt
- Subjects
Male ,Proband ,medicine.medical_specialty ,Visual acuity ,Adolescent ,genetic structures ,Ophthalmoparesis ,03 medical and health sciences ,0302 clinical medicine ,Retinal Diseases ,Ptosis ,Retinal Rod Photoreceptor Cells ,Physiology (medical) ,Ophthalmology ,Electroretinography ,medicine ,Humans ,medicine.diagnostic_test ,business.industry ,medicine.disease ,eye diseases ,Sensory Systems ,Hypotonia ,DNA Polymerase gamma ,Mutation ,030221 ophthalmology & optometry ,sense organs ,medicine.symptom ,business ,Erg ,Tomography, Optical Coherence ,030217 neurology & neurosurgery ,Retinopathy - Abstract
To report the clinical and novel electrophysiological features in a child with POLG-related sensory ataxic neuropathy, dysarthria and ophthalmoparesis (SANDO). The proband, a male child of Indian descent, underwent serial systemic and ophthalmological evaluations from birth until 14 years of age. Eye examinations included visual acuity and extraocular movement assessments, fundus photography, spectral domain optical coherence tomography and full-field electroretinography (ERG). Detailed genetic testing was also performed. The child carried a homozygous mutation in POLG (c.911T > G/p.Leu304Arg) and manifested systemic features such as seizures, headaches, areflexia, hypotonia, myopathy and vomiting. The child’s distance visual acuity was 0.50 and 0.40 LogMAR in the right and left eyes, respectively. Bilateral ophthalmoplegia and ptosis were observed at 5 years of age. The dark-adapted (DA) ERG responses to 2.29 cd s m−2 and 7.6 cd s m−2 stimuli showed a markedly reduced b/a ratio; an electronegative configuration was noted to a DA 7.6 ERG. This is the first documented case of an electronegative ERG in a POLG-related disorder consistent with generalized rod ON-bipolar dysfunction. The rest of the proband’s systemic and ophthalmological features were consistent with SANDO but some features overlapped with other POLG-related disorders such as Alpers–Huttenlocher syndrome and autosomal dominant progressive external ophthalmoplegia demonstrating the wide phenotypic overlap expected due to POLG mutations.
- Published
- 2020