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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

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-...

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Autores principales: Piecuch, Anna K., Skarżyński, Piotr H., Skarżyński, Henryk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10560793/
https://www.ncbi.nlm.nih.gov/pubmed/37786244
http://dx.doi.org/10.12659/AJCR.940439
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author Piecuch, Anna K.
Skarżyński, Piotr H.
Skarżyński, Henryk
author_facet Piecuch, Anna K.
Skarżyński, Piotr H.
Skarżyński, Henryk
author_sort Piecuch, Anna K.
collection PubMed
description 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 sensorineural hearing loss with auditory neuropathy. Surgical treatment was applied in the form of bilateral cochlear implantation. CONCLUSIONS: This report shows the importance of genetic testing in infants who present with atypical symptoms or signs. In this case, the diagnosis of Brown-Vialetto-Van Laere syndrome resulted in timely correction of the genetic riboflavin (vitamin B2) deficiency and improved hearing following the use of cochlear implants.
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spelling pubmed-105607932023-10-10 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 Piecuch, Anna K. Skarżyński, Piotr H. Skarżyński, Henryk Am J Case Rep Articles 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 sensorineural hearing loss with auditory neuropathy. Surgical treatment was applied in the form of bilateral cochlear implantation. CONCLUSIONS: This report shows the importance of genetic testing in infants who present with atypical symptoms or signs. In this case, the diagnosis of Brown-Vialetto-Van Laere syndrome resulted in timely correction of the genetic riboflavin (vitamin B2) deficiency and improved hearing following the use of cochlear implants. International Scientific Literature, Inc. 2023-10-03 /pmc/articles/PMC10560793/ /pubmed/37786244 http://dx.doi.org/10.12659/AJCR.940439 Text en © Am J Case Rep, 2023 https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Articles
Piecuch, Anna K.
Skarżyński, Piotr H.
Skarżyński, Henryk
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
title 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
title_full 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
title_fullStr 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
title_full_unstemmed 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
title_short 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
title_sort 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
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10560793/
https://www.ncbi.nlm.nih.gov/pubmed/37786244
http://dx.doi.org/10.12659/AJCR.940439
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