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A Case Report of Riboflavin Treatment and Cochlear Implants in a 4-Year-Old Girl with Progressive Hearing Loss and Delayed Speech Development: Brown-Vialetto-Van Laere Syndrome

Anna K Piecuch, P. Skarżyński, H. Skarżyńśki

The American journal of case reports, 2023

10 citations

Abstract

Patient: Female, 4-year-old Final Diagnosis: Brown-Vialetto-Van Laere syndrome Symptoms: Hearing loss auditory neuropathy • delayed speech development • pontobulbar palsy Clinical Procedure: Bilateral cochlear implantation Specialty: Otolaryngology Objective: Rare disease Background: Brown-Vialetto-Van Laere (BVVL) syndrome is a rare autosomal recessive disorder caused by mutations in intestinal riboflavin transporter genes, resulting in a motor neuron disorder of childhood, which can be associated with sensorineural deafness. This report describes a 4-year-old Polish girl with progressive hearing loss and delayed speech development diagnosed with Brown-Vialetto-Van Laere syndrome who was treated with riboflavin (vitamin B2) and cochlear implants. Case Report: The case report concerns a girl from Poland who, at the age of 2 years 10 months, developed progressive atypical neurological symptoms of unknown etiology: ataxia of the upper and lower limbs, gait abnormalities, generalized muscle weakness, visual and hearing problems, and regression of speech development. A karyotype study (whole-exome sequencing) revealed alterations within SLC52A2, leading to the diagnosis of Brown-Vialetto-Van Laere syndrome and initiation of high-dose riboflavin treatment. As a 4-year-old child, she presented to the Institute of Physiology and Pathology of Hearing – World Hearing Center in Poland with progressive hearing loss and speech regression. Hearing tests revealed bilateral profound…

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