Results 51 -
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Progressive encephalopathy
- ... people with a form of early-infantile epileptic encephalopathy (EIEE16; also called malignant migrating partial seizures of ... disorders, including familial infantile myoclonic epilepsy (FIME) and progressive myoclonus epilepsy (PME). These mutations likely result in ...
- ... of CLPB is associated with congenital microcephaly, severe encephalopathy and 3-methylglutaconic aciduria. J Med Genet. 2015 ... Wevers RA. CLPB mutations cause 3-methylglutaconic aciduria, progressive brain atrophy, intellectual disability, congenital neutropenia, cataracts, movement ...
- ... of CLPB is associated with congenital microcephaly, severe encephalopathy and 3-methylglutaconic aciduria. J Med Genet. 2015 ... Wevers RA. CLPB mutations cause 3-methylglutaconic aciduria, progressive brain atrophy, intellectual disability, congenital neutropenia, cataracts, movement ...
- ... have neurological problems, such as abnormal brain function (encephalopathy), recurrent seizures (epilepsy), intellectual disability, difficulty coordinating movements ( ...
- Liver Diseases (National Library of Medicine)Your liver is the largest organ inside your body. It helps your body digest food, store energy, and remove poisons. There are many kinds of liver diseases: ...
- American Liver Foundation (American Liver Foundation)... NAFLD) in Children Glycogen Storage Disease Type 1 Progressive Familial Intrahepatic Cholestasis (PFIC) Reye Syndrome Rare Liver ...
- Focus On Parkinson's Disease Research (National Institute of Neurological Disorders and Stroke)Parkinson's Disease/Statistics and Research ... Parkinson's Disease ... National Institute of Neurological Disorders and Stroke ... From the National Institutes of Health