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Results 81 - 90 of 133 for Optic nerve hypoplasia
  1. Rett syndrome 
    ... signs and symptoms that can develop include breathing abnormalities, spitting or drooling, unusual eye movements such as intense staring or excessive blinking, ...
    https://medlineplus.gov/genetics/condition/rett-syndrome - Genetics
  2. Autosomal dominant cerebellar ataxia, deafness, and narcolepsy 
    ... as the condition worsens include degeneration of the nerves that carry information from the eyes to the brain (optic atrophy); clouding of the ...
    https://medlineplus.gov/...cerebellar-ataxia-deafness-and-narcolepsy - Genetics
  3. Hypomyelination with brainstem and spinal cord involvement and leg spasticity 
    ... which is a group of conditions that involve abnormalities of the nervous system's white matter. The white matter consists of nerve fibers covered by a fatty substance, called myelin, ...
    https://medlineplus.gov/...pinal-cord-involvement-and-leg-spasticity - Genetics
  4. Pelizaeus-Merzbacher-like disease type 1 
    ... group of genetic disorders called leukodystrophies. Leukodystrophies are abnormalities of the nervous system's white matter, which consists of nerve fibers covered by a fatty substance called myelin. ...
    https://medlineplus.gov/.../pelizaeus-merzbacher-like-disease-type-1 - Genetics
  5. FBXL4-related encephalomyopathic mitochondrial DNA depletion syndrome 
    ... speech development. Many affected individuals have seizures, movement abnormalities, and an unusually small head size (microcephaly) with a loss of nerve cells in the brain (cerebral atrophy).All individuals ...
    https://medlineplus.gov/...thic-mitochondrial-dna-depletion-syndrome - Genetics
  6. RNAse T2-deficient leukoencephalopathy 
    ... brain. People with this condition have leukoencephalopathy, an abnormality of the brain's white matter that can be detected with medical imaging. White matter consists of nerve fibers covered by a fatty substance called myelin. ...
    https://medlineplus.gov/.../rnase-t2-deficient-leukoencephalopathy - Genetics
  7. Gyrate atrophy of the choroid and retina 
    ... Gyrate atrophy may also cause disturbances in the nerves connecting the brain and spinal cord to muscles and sensory cells (peripheral nervous system). In some people with the disorder these abnormalities lead to numbness, tingling, or pain in the ...
    https://medlineplus.gov/.../gyrate-atrophy-of-the-choroid-and-retina - Genetics
  8. Biotin-thiamine-responsive basal ganglia disease 
    ... inability to move facial muscles due to facial nerve paralysis (supranuclear facial palsy), paralysis of the eye muscles (external ophthalmoplegia), difficulty chewing or swallowing (dysphagia), ...
    https://medlineplus.gov/...thiamine-responsive-basal-ganglia-disease - Genetics
  9. Renpenning syndrome 
    ... or split in structures that make up the eye (coloboma), an opening in the roof of the mouth (cleft palate), heart abnormalities, or malformations of the anus.Certain combinations of ...
    https://medlineplus.gov/genetics/condition/renpenning-syndrome - Genetics
  10. Pelizaeus-Merzbacher disease 
    ... disorders called leukodystrophies. Leukodystrophies are conditions that involve abnormalities of the nervous system's white matter, which consists of nerve fibers covered by a fatty substance called myelin. ...
    https://medlineplus.gov/.../condition/pelizaeus-merzbacher-disease - Genetics
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