Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 28 for Progressive encephalopathy
  1. Tyrosine hydroxylase deficiency 
    ... Strassburg HM, Wevers RA. Tyrosine hydroxylase deficiency causes progressive encephalopathy and dopa-nonresponsive dystonia. Ann Neurol. 2003;54 ...
    https://medlineplus.gov/.../tyrosine-hydroxylase-deficiency - Genetics
  2. Asparagine synthetase deficiency 
    ... of asparagine synthetase causes congenital microcephaly and a progressive form of encephalopathy. Neuron. 2013 Oct 16;80(2):429-41. ...
    https://medlineplus.gov/.../asparagine-synthetase-deficiency - Genetics
  3. MECP2-related severe neonatal encephalopathy 
    ... J, Kaufmann WE, Ravine D, Percy AK. Early progressive encephalopathy in boys and MECP2 mutations. Neurology. 2006 Jul ...
    https://medlineplus.gov/...p2-related-severe-neonatal-encephalopathy - Genetics
  4. TH gene 
    ... Strassburg HM, Wevers RA. Tyrosine hydroxylase deficiency causes progressive encephalopathy and dopa-nonresponsive dystonia. Ann Neurol. 2003;54 ...
    https://medlineplus.gov/genetics/gene/th - Genetics
  5. Familial encephalopathy with neuroserpin inclusion bodies 
    ... inclusion bodies (FENIB) is a disorder that causes progressive dysfunction of the brain (encephalopathy). It is characterized by a loss of intellectual ...
    https://medlineplus.gov/...lopathy-with-neuroserpin-inclusion-bodies - Genetics
  6. Horizontal gaze palsy with progressive scoliosis 
    ... of the condition. Familial horizontal gaze palsy with progressive scoliosis Familial idiopathic scoliosis associated with congenital encephalopathy Familial infantile scoliosis associated with bilateral paralysis of ...
    https://medlineplus.gov/...tal-gaze-palsy-with-progressive-scoliosis - Genetics
  7. Acute necrotizing encephalopathy type 1 
    ... bleeding (hemorrhage), and then tissue death (necrosis). The progressive brain damage and tissue loss results in encephalopathy.Approximately one-third of individuals with acute necrotizing ...
    https://medlineplus.gov/.../acute-necrotizing-encephalopathy-type-1 - Genetics
  8. CSTB gene 
    ... believed to cause the signs and symptoms of progressive myoclonic epilepsy type 1, ... encephalopathy (abnormal brain function). These symptoms resemble those seen ...
    https://medlineplus.gov/genetics/gene/cstb - Genetics
  9. RRM2B gene 
    ... cells. MedlinePlus ... an eye condition called progressive external ophthalmoplegia. This disorder weakens the muscles that ...
    https://medlineplus.gov/genetics/gene/rrm2b - Genetics
  10. OPA1 gene 
    ... weakness in the muscles that control eye movement (progressive external ... dysfunction (encephalopathy), loss of sensation and weakness in the limbs ( ...
    https://medlineplus.gov/genetics/gene/opa1 - Genetics
previous · 1 · 2 · 3 · next