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Results 21 - 28 of 28 for Multiple sclerosis
  1. Gnathodiaphyseal dysplasia 
    ... fragile. As a result, affected individuals typically experience multiple ... and thick (diaphyseal sclerosis). Bowing of the long bones also occurs in ...
    https://medlineplus.gov/.../condition/gnathodiaphyseal-dysplasia - Genetics
  2. ALS2 gene 
    The ALS2 gene provides instructions for making a protein called alsin. Alsin is produced in a wide range of tissues, with highest amounts in the brain. This ...
    https://medlineplus.gov/genetics/gene/als2 - Genetics
  3. TARDBP gene 
    ... gene have been found to cause amyotrophic lateral sclerosis (ALS), a condition characterized by progressive muscle weakness, ... frontotemporal dementia (FTD) without features of amyotrophic lateral sclerosis (ALS, described above). FTD caused by TARDBP gene ...
    https://medlineplus.gov/genetics/gene/tardbp - Genetics
  4. SMN1 gene 
    ... down. MedlinePlus Genetics provides information about Amyotrophic lateral sclerosis More About This Health Condition Many mutations in ... with some people having up to eight copies. Multiple copies of the SMN2 gene are usually associated ...
    https://medlineplus.gov/genetics/gene/smn1 - Genetics
  5. ATXN2 gene 
    ... Condition MedlinePlus Genetics provides information about Amyotrophic lateral sclerosis More About This Health Condition ataxin-2 ATX2 ...
    https://medlineplus.gov/genetics/gene/atxn2 - Genetics
  6. Lennox-Gastaut syndrome 
    ... part of a genetic disorder, such as tuberous sclerosis complex. CHD2 FOXG1 SCN1A SCN8A STXBP1 Additional Information ...
    https://medlineplus.gov/genetics/condition/lennox-gastaut-syndrome - Genetics
  7. Neurofibromatosis type 1 
    ... a.31547. Citation on PubMed Kandt RS. Tuberous sclerosis complex and neurofibromatosis type 1: the two most ...
    https://medlineplus.gov/genetics/condition/neurofibromatosis-type-1 - Genetics
  8. Infantile-onset ascending hereditary spastic paralysis 
    ... this condition.A condition called juvenile primary lateral sclerosis shares many of the features of infantile-onset ... particularly in motor neurons. Alsin turns on (activates) multiple proteins called GTPases that convert a molecule called ...
    https://medlineplus.gov/...et-ascending-hereditary-spastic-paralysis - Genetics
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