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Results 1 - 10 of 10 for Troyer syndrome
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  1. Troyer syndrome 
    Troyer syndrome is a type of hereditary spastic paraplegia, also called hereditary spastic paraparesis. Hereditary spastic paraplegias are a group of genetic ...
    https://medlineplus.gov/genetics/condition/troyer-syndrome - Genetics
  2. Troyer Syndrome From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Leg Injuries and Disorders/Specifics ... Leg Injuries and Disorders ... Neuromuscular Disorders/Specifics ... Neuromuscular Disorders ... National Institute of Neurological ...
    https://www.ninds.nih.gov/.../disorders/troyer-syndrome - External Health Links
  3. SPART gene 
    ... also called mutations) in the SPART gene cause Troyer syndrome. Troyer syndrome is a type of hereditary spastic paraplegia (also ... leg muscles. The first known variant associated with Troyer syndrome was found in the Old Order Amish population ...
    https://medlineplus.gov/genetics/gene/spart - Genetics
  4. Neuromuscular Disorders (National Library of Medicine)  
    Neuromuscular disorders affect your neuromuscular system. They can cause problems with: The nerves that control your muscles Your muscles Communication between your ...
    https://medlineplus.gov/neuromusculardisorders.html - Health Topics
  5. Peripheral Nerve Disorders (National Library of Medicine)  
    What are peripheral nerves? Nerves are like wires that carry messages back and forth between your brain and your body. Your peripheral nerves branch off ...
    https://medlineplus.gov/peripheralnervedisorders.html - Health Topics
  6. Leg Injuries and Disorders (National Library of Medicine)  
    Your legs are made up of bones, blood vessels, muscles, and other connective tissue. They are important for motion and standing. Playing sports, running, ...
    https://medlineplus.gov/leginjuriesanddisorders.html - Health Topics
  7. Paralysis (National Library of Medicine)  
    Paralysis is the loss of muscle function in part of your body. It happens when something goes wrong with the way messages pass between your brain and muscles. ...
    https://medlineplus.gov/paralysis.html - Health Topics
  8. MN1 C-terminal truncation syndrome 
    ... meningioma National Organization for Rare Disorders (NORD) CEBALID SYNDROME; CEBALID PubMed Mak CCY, Doherty D, Lin AE, Vegas N, Cho MT, Viot G, Dimartino C, Weisfeld-Adams JD, Lessel D, Joss S, Li C, Gonzaga-Jauregui C, Zarate YA, Ehmke N, Horn D, Troyer C, Kant SG, Lee Y, Ishak GE, Leung ...
    https://medlineplus.gov/.../mn1-c-terminal-truncation-syndrome - Genetics
  9. MN1 gene 
    ... cells and are not inherited. People with MCTT syndrome do not appear to have an increased risk of leukemia. ... N, Cho MT, Viot G, Dimartino C, Weisfeld-Adams JD, Lessel D, Joss S, Li C, Gonzaga-Jauregui C, Zarate YA, Ehmke N, Horn D, Troyer C, Kant SG, Lee Y, Ishak GE, Leung ...
    https://medlineplus.gov/genetics/gene/mn1 - Genetics
  10. Mucopolysaccharidosis type II 
    ... D, Scearce-Levie K, Diaz D, Cahan H, Troyer MD, Harris JM, Escolar ML. Characterization of Fluid ... J. Recognition and diagnosis of mucopolysaccharidosis II (Hunter syndrome). Pediatrics. 2008 Feb;121(2):e377-86. doi: ...
    https://medlineplus.gov/.../condition/mucopolysaccharidosis-type-ii - Genetics