Alpers syndrome

Alpers syndrome, also known as Alpers-Huttenlocher syndrome or progressive cerebral poliodystrophy, is a rare childhood neurodegenerative POLG-related disorder. Along with Leigh syndrome, it is one of the commonest childhood mitochondrial disorders 1

Alpers syndrome is incredibly rare. The estimated prevalence is 1 per 100,000. 

Alpers syndrome generally affects infants within the first year of life, but cases have been reported later in childhood through to early adulthood 2-4. Affected individuals often present with severe, refractory status epilepticus 2. Loss of motor coordination, decreased muscle tone, cognitive decline, optic nerve atrophy, and hepatic impairment are often reported in disease progression 1,5

Autosomal recessive mutations in the DNA Polymerase Gamma, Catalytic Subunit (POLG) gene have been implicated in the majority of cases 5

Neuroimaging findings are most frequently described.

Findings are often subtle and include low densities in the cortex and white matter, especially in the occipital lobes, and cerebral atrophy 7.

Features described include:

  • regions of increased signal intensity on T2-weighted sequences and DWI, most often in the occipital lobes and thalami, involving both the cortex and deep gray matter 7-9
    • these regions often correspond to areas of pathological electroencephalogram (EEG) activity and may even be absent if no recent seizure activity has occurred 7-9
  • generalized cerebral atrophy, although may have an occipital preponderance 7-9
  • prior to development of POLG-related neurological manifestations, features of chronic hepatic encephalopathy, such as increased signal intensity on T1-weighted sequences in the globi pallidi and subthalamic regions, or acute hepatic encephalopathy may be seen 10
  • these features may be detected in prenatal MRI 8

MR spectroscopy may demonstrate an elevated lactate signal intensity and a reduced NAA signal intensity, in areas of high diffusion signal 10.

Treatment focuses on symptoms control. Sodium valproate as an agent for epilepsy control is generally avoided due to its hepatotoxicity which may result in rapid decline in liver function in patients with a predisposition to liver failure, such as those with Alpers syndrome 6.

Alpers syndrome often progresses rapidly, leading to death in childhood 5

Alpers syndrome was first described by Bernard Alpers in 1931 11. In the late 1970s, Peter Huttenlocher associated further patient phenotypes with that of Alpers' patient and the eponymous name was coined 12.

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Article information

rID: 66767
Section: Syndromes
Tag: cases
Synonyms or Alternate Spellings:
  • Progressive cerebral poliodystrophy
  • Alpers-Huttenlocher syndrome
  • Mitochondrial DNA depletion syndrome-4A

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