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DOI 10.3390/jcm15135289

Медицинская библиотека · Journal of clinical medicine · 2026

When LHON Mimics Demyelination: Area Postrema Syndrome in Biallelic DNAJC30 Variants.

Dzwilewski Kamil, Krygier Magdalena, Szymarek Jakub, Zawadzka Marta, Stodolska-Koberda Urszula, Mazurkiewicz-Bełdzińska Maria

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Аннотация

Introduction

Biallelic pathogenic variants in DNAJC30 cause an autosomal recessive form of Leber hereditary optic neuropathy (LHONAR1), traditionally considered a mitochondrially transmitted disorder. The phenotypic spectrum of diseases linked to DNAJC30 includes isolated optic neuropathy, Leigh syndrome spectrum (LSS), and atypical LHON-plus. Case description: Here, we report a 13-year-old boy presenting symptoms of area postrema syndrome (APS), with recurrent vomiting, vertigo, nystagmus, and subacute visual deterioration with central scotoma. Ophthalmological examination revealed bilateral papilledema with telangiectatic vessels, while visual evoked potentials demonstrated severe bilateral optic pathway dysfunction. Brain magnetic resonance imaging (MRI) showed T2/FLAIR hyperintense lesions involving the area postrema and enhancement of the optic nerves, strongly suggesting seronegative neuromyelitis optica spectrum disorder (NMOSD). Extensive immunological and cerebrospinal fluid studies, including anti-aquaporin-4 (AQP4) and anti-MOG antibodies, were negative. High-dose corticosteroids and intravenous immunoglobulins resulted in only transient and incomplete improvement, followed by further visual decline. Additionally, laboratory tests detected elevated lactate plasma levels. Hence, whole-exome sequencing was performed, which identified a homozygous pathogenic DNAJC30 c.152A>G, p.(Tyr51Cys) variant, associated with LHONAR1. After initiation of idebenone therapy, the patient showed significant improvement in visual function, normalization of lactate levels, and complete resolution of the brainstem lesions on follow-up MRI.

Conclusions

This case further expands the neuro-ophthalmic spectrum associated with DNAJC30 variants and suggests that DNAJC30-related disease may closely mimic seronegative NMOSD. We highlight that early genetic diagnosis is essential, as recognition of this mitochondrial etiology enables targeted therapy and may substantially improve clinical outcomes.

Для цитирования: Dzwilewski Kamil, Krygier Magdalena, Szymarek Jakub, Zawadzka Marta, Stodolska-Koberda Urszula, Mazurkiewicz-Bełdzińska Maria. When LHON Mimics Demyelination: Area Postrema Syndrome in Biallelic DNAJC30 Variants.. Journal of clinical medicine. 2026. DOI: 10.3390/jcm15135289.
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