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Results 1 - 9 of 9 for Acute encephalopathy
  1. Acute necrotizing encephalopathy type 1 
    ... 1, also known as susceptibility to infection-induced acute encephalopathy 3 or IIAE3, is a rare type of ... to acute necrotizing encephalopathy Susceptibility to infection-induced acute encephalopathy Susceptibility to infection-induced acute encephalopathy 3 Genetic ...
    https://medlineplus.gov/.../acute-necrotizing-encephalopathy-type-1 - Genetics
  2. Carbonic anhydrase VA deficiency 
    ... crisis) and brain function is abnormal (known as acute encephalopathy). These potentially life-threatening episodes can cause poor ... their age.The risk of metabolic crisis and acute encephalopathy is thought to decrease after childhood. Because of ...
    https://medlineplus.gov/.../carbonic-anhydrase-va-deficiency - Genetics
  3. RANBP2 gene 
    ... condition, also known as susceptibility to infection-induced acute encephalopathy 3 or IIAE3, is a rare type of ... viral infection triggers neurological damage. While individuals with acute necrotizing encephalopathy type 1 frequently have damage to and often ...
    https://medlineplus.gov/genetics/gene/ranbp2 - Genetics
  4. Alpha-methylacyl-CoA racemase deficiency 
    ... decline), seizures, and migraines. They may also have acute episodes of brain dysfunction (encephalopathy) similar to stroke, involving altered consciousness and areas ...
    https://medlineplus.gov/.../alpha-methylacyl-coa-racemase-deficiency - Genetics
  5. Carnitine palmitoyltransferase I deficiency 
    ... are at risk of developing a condition called acute fatty liver of pregnancy (AFLP). AFLP begins with ...
    https://medlineplus.gov/...rnitine-palmitoyltransferase-i-deficiency - Genetics
  6. Leigh syndrome 
    ... and these problems can worsen until they cause acute respiratory failure. Some affected individuals develop hypertrophic cardiomyopathy, ... family history of this condition. Infantile subacute necrotizing encephalopathy Juvenile subacute necrotizing encephalopathy Leigh disease Leigh's ...
    https://medlineplus.gov/genetics/condition/leigh-syndrome - Genetics
  7. N-acetylglutamate synthase deficiency 
    ... in the N-acetylglutamate synthase gene associated with acute neonatal disease and hyperammonemia. Hum Genet. 2003 Apr; ... acetylglutamate synthase deficiency and the treatment of hyperammonemic encephalopathy. Ann Neurol. 2002 Dec;52(6):845-9. ...
    https://medlineplus.gov/.../n-acetylglutamate-synthase-deficiency - Genetics
  8. Chromosome 5 
    ... developing a fast-growing blood cancer known as acute myeloid leukemia (AML).Most people with 5q- syndrome ... in PURA cause profound neonatal hypotonia, seizures, and encephalopathy in 5q31.3 microdeletion syndrome. Am J Hum ...
    https://medlineplus.gov/genetics/chromosome/5 - Genetics
  9. Intestinal pseudo-obstruction 
    ... intestinal pseudo-obstruction. The condition can be episodic (acute) or persistent (chronic). The overall prevalence of intestinal ... microcolon-intestinal hypoperistalsis syndrome (MMIHS) or mitochondrial neurogastrointestinal encephalopathy disease (MNGIE disease). Infections, surgery, or certain drugs ...
    https://medlineplus.gov/.../condition/intestinal-pseudo-obstruction - Genetics