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Results 1 - 4 of 4 for Progressive bulbar palsy
  1. Riboflavin transporter deficiency neuronopathy 
    ... disease 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 
    ... Boyd 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 
    ... hereditary spastic paraplegias. These disorders are characterized by progressive muscle stiffness (spasticity) and eventual paralysis of the lower limbs (paraplegia). The spasticity and ...
    https://medlineplus.gov/...et-ascending-hereditary-spastic-paralysis - Genetics