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Results 1 - 6 of 6 for Spastic paraplegia 35
  1. Fatty acid hydroxylase-associated neurodegeneration 
    ... classified as having a separate disorder called spastic paraplegia 35. People with mutations in this gene resulting in ... condition. Dysmyelinating leukodystrophy and spastic paraparesis FAHN Spastic paraplegia 35 Genetic Testing Registry: Hereditary spastic paraplegia 35 Fatty ...
    https://medlineplus.gov/...-hydroxylase-associated-neurodegeneration - Genetics
  2. FA2H gene 
    ... classified as having a separate disorder called spastic paraplegia 35. People with mutations in this gene resulting in ... hydroxylase domain containing 1 FAXDC1 FLJ25287 SCS7 spastic paraplegia 35 (autosomal recessive) SPG35 Tests of FA2H PubMed FATTY ...
    https://medlineplus.gov/genetics/gene/fa2h - Genetics
  3. Spastic paraplegia type 3A 
    ... Central Blackstone C. Cellular pathways of hereditary spastic paraplegia. Annu Rev Neurosci. 2012;35:25-47. doi: 10.1146/annurev-neuro-062111- ...
    https://medlineplus.gov/.../condition/spastic-paraplegia-type-3a - Genetics
  4. Muscle function loss 
    ... the body and both legs it is called paraplegia. If it affects both arms and legs, it ... Orthopaedics. 14th ed. Philadelphia, PA: Elsevier; 2021:chap 35.
    https://medlineplus.gov/ency/article/003190.htm - Medical Encyclopedia
  5. Pelizaeus-Merzbacher disease 
    ... of myelination and atrophy on cerebral imaging in 35 patients with PLP1-related disorders. Dev Med Child ...
    https://medlineplus.gov/.../condition/pelizaeus-merzbacher-disease - Genetics
  6. PNP gene 
    ... deoxyguanosine to another molecule called guanine. More than 35 PNP gene mutations have been identified in individuals ... nucleoside phosphorylase deficiency in a patient with spastic paraplegia and recurrent infections. J Child Neurol. 2007 Jun; ...
    https://medlineplus.gov/genetics/gene/pnp - Genetics