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Results 1 - 10 of 10 for Infantile neuroaxonal dystrophy
  1. ... Seitelberger's disease Genetic Testing Registry: Infantile neuroaxonal dystrophy Infantile neuroaxonal dystrophy National Organization for Rare Disorders (NORD) ClinicalTrials. ...
  2. Infantile Neuroaxonal Dystrophy From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Genetic Disorders/Specifics ... Genetic Disorders ... Degenerative Nerve Diseases/Specifics ... Degenerative Nerve Diseases ... Optic Nerve Disorders/Specifics ... Optic Nerve ...
  3. ... glycoaminoacid storage disease-angiokeratoma corporis diffusum NAGA deficiency Neuroaxonal dystrophy, Schindler type Neuronal axonal dystrophy, Schindler type Genetic ...
  4. ... gene have been identified in people with infantile neuroaxonal dystrophy, a progressive neurological disorder that causes intellectual disability ... lead to the signs and symptoms of infantile neuroaxonal dystrophy, phospholipid metabolism problems have been seen in both ...
  5. Degenerative Nerve Diseases (National Library of Medicine)  
    Degenerative nerve diseases affect many of your body's activities, such as balance, movement, talking, breathing, and heart function. Many of these diseases are genetic. ...
  6. Genetic Disorders (National Library of Medicine)  
    Genes are the building blocks of heredity. They are passed from parent to child. They hold DNA, the instructions for making proteins. Proteins do most of the ...
  7. Optic Nerve Disorders (National Library of Medicine)  
    The optic nerve is a bundle of more than 1 million nerve fibers that carry visual messages. You have one connecting the back of each eye (your retina) to ...
  8. ... in certain other neurological disorders such as infantile neuroaxonal dystrophy and pantothenate kinase-associated neurodegeneration. All these conditions ...
  9. ... OSTEOPETROSIS, AUTOSOMAL DOMINANT 2; OPTA2 OSTEOPETROSIS AND INFANTILE NEUROAXONAL DYSTROPHY OSTEOPETROSIS, AUTOSOMAL RECESSIVE 1; OPTB1 OSTEOPETROSIS, AUTOSOMAL RECESSIVE ...
  10. ... Desnick RJ, Wang AM. Schindler disease: an inherited neuroaxonal dystrophy due to alpha-N-acetylgalactosaminidase deficiency. J Inherit ...