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Results 71 - 80 of 90 for Brain atrophy
  1. Pelizaeus-Merzbacher disease 
    ... Boespflug-Tanguy O. Time-course of myelination and atrophy on cerebral imaging in 35 patients with PLP1- ... mutations in Chinese patients with Pelizaeus-Merzbacher disease. Brain Dev. 2015 Sep;37(8):797-802. doi: ...
    https://medlineplus.gov/.../condition/pelizaeus-merzbacher-disease - Genetics
  2. Myotonic dystrophy 
    ... the correct functioning of cells in the heart, brain, and skeletal muscles (which are used for movement). ...
    https://medlineplus.gov/genetics/condition/myotonic-dystrophy - Genetics
  3. GRN-related frontotemporal lobar degeneration 
    ... H, Wszolek ZK, Kantarci K. Trajectory of lobar atrophy in asymptomatic and symptomatic GRN mutation carriers: a ... carriers: a clinical, neuropsychological, imaging and genetic study. Brain. 2008 Mar;131(Pt 3):732-46. doi: ...
    https://medlineplus.gov/...related-frontotemporal-lobar-degeneration - Genetics
  4. SUCLA2-related mitochondrial DNA depletion syndrome 
    ... include uncontrolled movements (dystonia), hearing loss, muscle wasting (atrophy), and intellectual disabilities. In most affected children, a ... methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness. Brain. 2007 Mar;130(Pt 3):862-74. doi: ...
    https://medlineplus.gov/...ated-mitochondrial-dna-depletion-syndrome - Genetics
  5. Aceruloplasminemia 
    ... small opaque spots and areas of tissue degeneration (atrophy) around the edges of the retina. These abnormalities ... Gitlin JD. Copper and iron disorders of the brain. Annu Rev Neurosci. 2007;30:317-37. doi: ...
    https://medlineplus.gov/genetics/condition/aceruloplasminemia - Genetics
  6. Microcephaly, seizures, and developmental delay 
    ... Spek P, Kremer A, Mancini GM. Progressive cerebellar atrophy and polyneuropathy: expanding the spectrum of PNKP mutations. ...
    https://medlineplus.gov/...ocephaly-seizures-and-developmental-delay - Genetics
  7. Pelizaeus-Merzbacher-like disease type 1 
    ... 1 have normal intelligence. Rarely, hearing loss, optic atrophy, and recurrent seizures (epilepsy) can occur. The prevalence ... These changes lead to nerve damage in the brain and spinal cord that impairs nervous system function, ...
    https://medlineplus.gov/.../pelizaeus-merzbacher-like-disease-type-1 - Genetics
  8. McLeod neuroacanthocytosis syndrome 
    ... muscles, including muscle weakness (myopathy) and muscle degeneration (atrophy). Sometimes, nerves that connect to muscles atrophy (neurogenic atrophy), leading to loss of muscle mass ...
    https://medlineplus.gov/.../mcleod-neuroacanthocytosis-syndrome - Genetics
  9. LMNA-related congenital muscular dystrophy 
    ... cause weak muscle tone (hypotonia) and muscle wasting (atrophy) beginning very early in life.In people with ... muscle cells and lead to muscle weakness and atrophy in people with L-CMD. LMNA L-CMD ...
    https://medlineplus.gov/...mna-related-congenital-muscular-dystrophy - Genetics
  10. Dihydropyrimidinase deficiency 
    ... cyclic vomiting). Affected individuals can also have deterioration (atrophy) of the small, finger-like projections (villi) that ... which to absorb nutrients. This condition, called villous atrophy, can lead to difficulty absorbing nutrients from foods ( ...
    https://medlineplus.gov/.../condition/dihydropyrimidinase-deficiency - Genetics
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