Brown–Vialetto–Van Laere Syndrome: A Rare, Potentially Treatable Neurometabolic Disorder!

Author:

Parida Swati1,Kumar Anand1,Singh Varun Kumar1,Pattanayak Sabyasachi1,Khatri Aparna1,Joshi Deepika1

Affiliation:

1. Department of Neurology, Institute of Medical Sciences, Banaras Hindu University, Varanasi, Uttar Pradesh, India

Publisher

Medknow

Subject

Neurology (clinical),Neurology

Reference9 articles.

1. Brown-Vialetto-Van Laere syndrome:A rare case report of MND mimic;Kranthi;Neurol India,2020

2. Clinical presentation and outcome of riboflavin transporter deficiency:Mini review after five years of experience;Jaeger;J Inherit Metab Dis,2016

3. Brown-Vialetto-Van Laere syndrome, a ponto-bulbar palsy with deafness, is caused by mutations in c20orf54;Green;Am J Hum Genet,2010

4. Infantile amyotrophic lateral sclerosis of the familial type;Brown;J Nerv Ment Dis,1894

5. Contributo alla forma ereditaria della paralisi bulb are progressive;Vialetto;Riv Sper Freniat,1936

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