210 top medical experts on Brown-Vialetto-Van Laere syndrome across 23 countries and 8 U.S. states, including 31 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Brown-Vialetto-Van Laere syndrome: A rare, genetic motor neuron disease characterized by a peripheral and cranial neuropathy, neuronal loss in anterior horns and atrophy of spinal sensory tracts, causing muscle weakness, sensory loss, diaphragmatic paralysis and respiratory insufficiency, and multiple cranial nerve deficits such as sensorineural hearing loss, bulbar symptoms, and loss of vision due to optic atrophy. Depending on the transporter affected, Riboflavin transporter deficiency 2 (RFVT2) and Riboflavin transporter deficiency 3 (RFVT3) are distinguished.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Support Organizations
  4. Synonyms: With Sensorineural Deafness Progressive Bulbar Palsy,  Pontobulbar Palsy With Deafness,  Pontobulbar palsy and neurosensory deafness,  Progressive Bulbar Palsy with Sensorineural Deafness


  

        

                    


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