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Results 1 - 10 of 39 for Spastic paraplegia 3
  1. Spastic paraplegia type 3A 
    ... inherits the mutation from one affected parent. Spastic paraplegia 3 Spastic paraplegia 3A SPG3A Genetic Testing Registry: Hereditary ... Organization for Rare Disorders (NORD) ClinicalTrials.gov SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT; SPG3A PubMed Alvarez V, Sanchez-Ferrero ...
    https://medlineplus.gov/.../condition/spastic-paraplegia-type-3a - Genetics
  2. Kallmann syndrome 
    ... OR WITHOUT ANOSMIA; HH1 KALLMANN SYNDROME WITH SPASTIC PARAPLEGIA HYPOGONADOTROPIC HYPOGONADISM 3 WITH OR WITHOUT ANOSMIA; HH3 HYPOGONADOTROPIC HYPOGONADISM 4 ...
    https://medlineplus.gov/genetics/condition/kallmann-syndrome - Genetics
  3. Traumatic Spinal Cord Injury Facts and Figures at a Glance (University of Alabama at Birmingham) - PDF  
    Spinal Cord Injuries/Statistics and Research ... Spinal Cord Injuries ... University of Alabama at Birmingham ... PDF
    https://www.nscisc.uab.edu/public/Facts and Figures 2024 - Final.pdf - External Health Links
  4. Spastic paraplegia type 31 
    ... one to 12 per 100,000 individuals. Spastic paraplegia type 31 accounts for 3 to 9 percent of all autosomal dominant hereditary spastic paraplegia cases. Spastic paraplegia type 31 is caused by ...
    https://medlineplus.gov/.../condition/spastic-paraplegia-type-31 - Genetics
  5. OPA3 gene 
    ... MGA3 MGC75494 OPA3 protein OPA3_HUMAN optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia) Tests of OPA3 PubMed OUTER MITOCHONDRIAL MEMBRANE LIPID ...
    https://medlineplus.gov/genetics/gene/opa3 - Genetics
  6. GJC2 gene 
    ... GAP JUNCTION PROTEIN, GAMMA-2; GJC2 LYMPHATIC MALFORMATION 3; LMPHM3 SPASTIC PARAPLEGIA 44, AUTOSOMAL RECESSIVE; SPG44 NCBI Gene ClinVar Gotoh L, Inoue K, Helman G, Mora S, Maski K, Soul JS, Bloom M, Evans SH, Goto YI, ... Mol Genet Metab. 2014 Mar;111(3):393-398. doi: 10.1016/j.ymgme.2013. ...
    https://medlineplus.gov/genetics/gene/gjc2 - Genetics
  7. Spastic paraplegia type 11 
    ... encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum. Nat Genet. 2007 Mar;39(3):366-72. doi: 10.1038/ng1980. Epub 2007 ...
    https://medlineplus.gov/.../condition/spastic-paraplegia-type-11 - Genetics
  8. SPG11 gene 
    ... encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum. Nat Genet. 2007 Mar;39(3):366-72. doi: 10.1038/ng1980. Epub 2007 ...
    https://medlineplus.gov/genetics/gene/spg11 - Genetics
  9. Purine nucleoside phosphorylase deficiency 
    ... nucleoside phosphorylase deficiency in a patient with spastic paraplegia and recurrent infections. J Child Neurol. 2007 Jun;22(6):741-3. doi: 10.1177/0883073807302617. Citation on PubMed Somech ...
    https://medlineplus.gov/...urine-nucleoside-phosphorylase-deficiency - Genetics
  10. PNP gene 
    ... nucleoside phosphorylase deficiency in a patient with spastic paraplegia and recurrent infections. J Child Neurol. 2007 Jun;22(6):741-3. doi: 10.1177/0883073807302617. Citation on PubMed Somech ...
    https://medlineplus.gov/genetics/gene/pnp - Genetics
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