Nl-Fr

View abstract

This abstract is assigned to sessions
Presentation typeE-poster
TitleBeyond mitochondrial DNA: a POLG-related LHON phenotype
PurposeTo describe a patient with a LHON phenotype associated with POLG variants.
MethodsComprehensive ophthalmic examination, retinal imaging, visual field and colour vision testing, brain MRI, biochemical and genetic investigations were performed.
ResultsA 25-year-old woman presented with subacute bilateral visual loss progressing over four months to counting fingers in both eyes. Visual fields showed bilateral central scotomata. Colour vision was absent. OCT demonstrated progressive thinning of the ganglion cell layer and temporal retinal nerve fibre layer, consistent with optic atrophy. Fundus examination revealed bilateral temporal optic disc pallor. Brain MRI showed no abnormalities explaining the visual loss, although nonspecific white matter changes greater than expected for age were present. Four months later, progressive sensorineural hearing loss developed. Mitochondrial DNA sequencing, biotinidase activity, anti-MOG, anti-AQP4 and paraneoplastic antibody testing were negative. Whole-exome sequencing identified two POLG variants: c.752C>T, p.(Thr251Ile) and c.1760C>T, p.(Pro587Leu).
ConclusionPOLG-related disease may present as a classic LHON phenotype. Nuclear mitochondrial genes, including POLG, should therefore be considered in patients with suspected LHON, particularly when extraocular features such as hearing loss are present.
Conflict of interestNo
Authors 1
Last nameBERGHMANS
InitialsL
DepartmentDepartment of Ophthalmology, Ghent University Hospital
CityGhent
Authors 2
Last nameDE BAERE
InitialsE
DepartmentDepartment of Medical Genetics, Ghent University Hospital
CityGhent
Authors 3
Last namePOPPE
InitialsB
DepartmentDepartment of Medical Genetics, Ghent University Hospital
CityGhent
Authors 4
Last nameHEMELSOET
InitialsD
DepartmentDepartment of Neurology, Ghent University Hospital
CityGhent
Authors 5
Last nameVAN DE SOMPELE
InitialsS
DepartmentDepartment of Medical Genetics, Ghent University Hospital
CityGhent
Authors 6
Last nameDE ZAEYTIJD
InitialsJ
DepartmentDepartment of Ophthalmology, Ghent University Hospital
CityGhent
top ^