Leber Mitochondrial Optic Neuropathy in Pediatric Females With Focus on Very Early Onset Cases

Author:

Tagliani Sara1ORCID,Malaventura Cristina1ORCID,Ceccato Chiara2,Parmeggiani Francesco34,Suppiej Agnese124ORCID

Affiliation:

1. Department of Medical Sciences, Pediatric Section, University Hospital of Ferrara, Ferrara, Italy

2. Robert Hollman Foundation, Padova, Italy

3. Department of Translational Medicine and for Romagna, University of Ferrara, Ferrara, Italy

4. ERN-EYE Network – Center for Retinitis Pigmentosa of Veneto Region, Camposampiero Hospital, Padova, Italy

Abstract

The aim of this study was to describe the phenotype of Leber hereditary optic neuropathy occurring in pediatric females. This disease generally affects young adult males, but it can occur also in females, and research data in this population is lacking. The very early onset can challenge the diagnosis and delay treatment. We searched PubMed through February 2021 and identified 226 pediatric females with genetically confirmed Leber hereditary optic neuropathy and added a new case of a 3-year-old female. The male-female ratio was 1.8:1; the mean onset age in females was 11 years with the onset at 3 years of age occurring in 3 females only. Acute onset with mild visual impairment was the most common presentation, associated with optic disc edema in 16%. Differential diagnoses are pseudotumor cerebri, optic nerve drusen and optic neuritis. The outcome is poor with partial recovery in 50%, despite some receiving Idebenone therapy.

Publisher

SAGE Publications

Subject

Neurology (clinical),Pediatrics, Perinatology and Child Health

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