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Results 1 - 4 of 4 for Bulbar palsy
  1. Riboflavin transporter deficiency neuronopathy 
    ... Fazio-Londe syndrome Pontobulbar palsy with deafness Progressive bulbar palsy with sensorineural deafness Riboflavin transporter deficiency Genetic Testing ...
    https://medlineplus.gov/...lavin-transporter-deficiency-neuronopathy - Genetics
  2. SLC52A3 gene 
    ... DJ. Brown-Vialetto-Van Laere syndrome, a ponto-bulbar palsy with deafness, is caused by mutations in c20orf54. ... S, Harding B, Brett EM, Wilson J. Progressive bulbar paralysis of childhood. A reappraisal of Fazio-Londe disease. ...
    https://medlineplus.gov/genetics/gene/slc52a3 - Genetics
  3. ALS2 gene 
    ... a homogeneous phenotype of infantile-onset ascending spastic paralysis with bulbar involvement in two siblings. Clin Genet. 2003 Sep;64(3):210-5. doi: 10.1034/j.1399-0004.2003.00138.x. Citation on PubMed ... hereditary spastic paralysis is associated with mutations in the alsin gene. ...
    https://medlineplus.gov/genetics/gene/als2 - Genetics
  4. Infantile-onset ascending hereditary spastic paralysis 
    ... S. Infantile-onset ascending hereditary spastic paraplegia with bulbar involvement due to the novel ALS2 mutation c.2761C>T. Gene. 2014 Feb 15;536(1):217-20. doi: 10.1016/j.gene.2013.11.043. Epub 2013 Dec 4. Citation on PubMed
    https://medlineplus.gov/...et-ascending-hereditary-spastic-paralysis - Genetics