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Results 31 - 39 of 39 for Brain atrophy
  1. ANO5 gene 
    ... related disorders characterized by muscle weakness and wasting (atrophy), particularly in the shoulders, hips, thighs, and upper ... disorder that is characterized by progressive weakness and atrophy of muscles that are away from the center ...
    https://medlineplus.gov/genetics/gene/ano5 - Genetics
  2. PNKP gene 
    ... Spek P, Kremer A, Mancini GM. Progressive cerebellar atrophy and polyneuropathy: expanding the spectrum of PNKP mutations. ...
    https://medlineplus.gov/genetics/gene/pnkp - Genetics
  3. DMD gene 
    ... are characterized by progressive muscle weakness and wasting (atrophy) and a heart condition called dilated cardiomyopathy. Most ... Anderson JL, Head SI, Rae C, Morley JW. Brain function in Duchenne muscular dystrophy. Brain. 2002 Jan; ...
    https://medlineplus.gov/genetics/gene/dmd - Genetics
  4. EXOSC3 gene 
    ... with intellectual disability, early onset spasticity, and cerebellar atrophy detects a novel mutation in EXOSC3. Neurogenetics. 2013 ...
    https://medlineplus.gov/genetics/gene/exosc3 - Genetics
  5. ALS2 gene 
    ... of axons and dendrites, contribute to the progressive atrophy of motor neurons that is characteristic of this ... JPLS reveals new aspects of alsin biological function. Brain. 2006 Jul;129(Pt 7):1710-9. doi: ...
    https://medlineplus.gov/genetics/gene/als2 - Genetics
  6. VRK1 gene 
    ... M, King MC, Levy-Lahad E. Spinal muscular atrophy with pontocerebellar hypoplasia is caused by a mutation ...
    https://medlineplus.gov/genetics/gene/vrk1 - Genetics
  7. POLR3A gene 
    ... leukodystrophy with oligodontia (LO); or hypomyelination with cerebellar atrophy and hypoplasia of the corpus callosum (HCAHC). Because ... frequent cause of sporadic and recessive spastic ataxia. Brain. 2017 Jun 1;140(6):1561-1578. doi: ...
    https://medlineplus.gov/genetics/gene/polr3a - Genetics
  8. DCTN1 gene 
    ... KH, Ludlow CL. Distal spinal and bulbar muscular atrophy caused by dynactin mutation. Ann Neurol. 2005 May; ...
    https://medlineplus.gov/genetics/gene/dctn1 - Genetics
  9. COQ8B gene 
    ... in CABC1/ADCK3 cause progressive cerebellar ataxia and atrophy. Mitochondrion. 2010 Aug;10(5):510-5. doi: ...
    https://medlineplus.gov/genetics/gene/coq8b - Genetics
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