Results 1 - 10 of 11 for Ceroid lipofuscinosis neuronal 10
  1. ... deficient neuronal ceroid lipofuscinosis cathepsin D CLN10 neuronal ceroid lipofuscinosis 10 neuronal ceroid lipofuscinosis due to cathepsin D deficiency For ...
  2. Neuronal ceroid lipofuscinoses (NCLS) refers to a group of rare, inherited disorders of the nerve cells. There are three ... Elsevier; 2011:chap 592. Mole SE, Williams RE. Neuronal Ceroid-Lipofuscinoses. In: Pagon RA, Adam MP, Bird TD, eds. ...
  3. Genetics Home Reference: Northern epilepsy From the National Institutes of Health (National Library of Medicine)  
    ... Gene Review: Neuronal Ceroid-Lipofuscinoses Genetic Testing Registry: Ceroid lipofuscinosis, neuronal, 8, northern epilepsy variant You might also find ...
  4. ... problems Seizures Mental disability Lung problems Early Infantile Neuronal Ceroid Lipofuscinosis Early infantile NCL appears in the first year ... disability. Children with severe Hunter syndrome often live 10 to 20 years. The mild form usually starts ...
  5. Genetics Home Reference: Kufs disease From the National Institutes of Health (National Library of Medicine)  
    ... Registry: Adult neuronal ceroid lipofuscinosis Genetic Testing Registry: Ceroid lipofuscinosis neuronal 4B autosomal dominant You might also find information ...
  6. Rare Diseases and Related Terms From the National Institutes of Health (Office of Rare Diseases)  
    ... See Liver cancer * Adult NCL - See Adult neuronal ceroid lipofuscinosis * Adult neuronal ceroid lipofuscinosis * Adult neuronal ceroid lipofuscinosis 4B - See Autosomal dominant neuronal ceroid ...
  7. National Institute of Neurological Disorders and Stroke (National Institute of Neurological Disorders and Stroke)  
    ... Neurological Sequelae Of Lupus Neuromyelitis Optica Neuromyotonia Neuronal Ceroid Lipofuscinosis Neuronal Migration Disorders Neuropathy - Hereditary Neurosarcoidosis Neurotoxicity Nevus Cavernosus ...
  8. Rare Diseases Clinical Research Network (Rare Diseases Clinical Research Network)  
    ... syndrome I-cell disease Krabbe disease Late Infantile Neuronal Ceroid Lipofuscinosis Maroteaux-Lamy syndrome Metachromatic leukodystrophy Morquio syndrome Mucolipidosis ...
  9. What Is Batten Disease (Batten Disease Support and Research Association)  
    ... and is sometimes called Haltia-Santavuori Disease, Infantile neuronal ceroid lipofuscinoses, or INCL. How does the disease progress? Genotype/ ... seizures (average age of onset of seizures is 10 years). Often the first seizures are motor seizures ...
  10. Genetic Brain Disorders (National Library of Medicine)  
    A genetic brain disorder is caused by a variation or a mutation in a gene. A variation is a different form of a gene. A mutation is a change in a gene. ...
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