Aicardi-Goutières syndrome

Aicardi-Goutières syndrome is a rare hereditary neurodegenerative disease which usually presents in early infancy with systemic and central nervous system inflammatory syndrome characterized by hepatosplenomegaly, vasculopathy and encephalopathy. Many of the features are similar to congenital TORCH infections.


Evidence suggests that familial systemic lupus erythematosus and microcephaly-intracranial calcification syndrome (MICS) - also known as pseudo-TORCH syndrome or Baraitser-Reardon syndrome are in fact phenotypic variants of Aicardi-Goutières syndrome.

Note: Aicardi-Goutières syndrome is distinct from Aicardi syndrome.


Aicardi-Goutières syndrome is rare and usually inherited in an autosomal recessive pattern (see pathology below). Penetrance is variable as is the age of clinical onset; most within the first year of life (3 - 7 months is typical) although delayed onset in later childhood is reported .

Clinical presentation

Aicardi-Goutières syndrome has variable penetrance with some individuals being only mildly affected. The majority, however, present with both physical and intellectual disabilities in infancy after a period of apparently normal development (often only lasting a few weeks).

Presentation may be with:

  • neurological
    • developmental delay and regression
    • irritability
    • ocular and myoclonic jerks
    • seizures (25%)
  • small head size
  • intermittent pyrexias
  • hepatosplenomegaly
  • abnormal liver enzymes
  • thrombocytopenia
  • chilblain of the fingers/toes and ears

During the active phase of the disease, elevation of interferon-α levels and a lymphocytosis can be detected in the CSF .


Aicardi-Goutières syndrome is the result of a number of genetic mutations. These usually, but not invariably, demonstrate autosomal recessive inheritance .

Multiple genes have been identified including:

  • autosomal recessive or dominant: ADAR, TREX1 (common)
  • autosomal recessive: RNASEH2A, RNASEH2B (most common), RNASEH2C, SAMHD1
  • autosomal dominant: IFIH1

The exact pathogenesis has not been fully understood. However, it appears to be the result of impaired metabolism/clearance of cellular nucleic acid debris. Accumulation eventually triggers an immune response with ensuing damage to various tissues similar to that seen in antenatal infections (e.g. TORCH) and autoimmune diseases (e.g. systemic lupus erythematosus) .

Radiographic features


Calcification of basal ganglia, thalamus and paraventricular white matter . The morphology of the calcification varies greatly from large 'chunks' of dense calcification to tiny punctate specks .


High T2 signal in the white matter, especially in the frontal and temporal lobes surrounding the ventricular horns . Temporal lobe cysts-like spaces may also form .

Over time, atrophy develops, particularly of the periventricular regions . The brainstem and cerebellum may also develop prominent atrophy .

Arteriopathy is also a prominent feature of SAMHD1 mutations with aneurysms, stenoses and moyamoya pattern encountered.

Treatment and prognosis

Although no established treatment exists, there is evidence that immune modulation (e.g. corticosteroids) during the active phase of the disease may be of benefit.

Although not established beyond doubt, it appears that Aicardi-Goutières syndrome represents a monophasic encephalopathy in infancy without ongoing progression. Death is therefore believed to be the consequence of neurological damage that occurred during the active phase of the disease rather than representing true disease progression.

History and etymology

Named after the French pediatric neurologists Jean Aicardi (1926-2015) and Francoise Goutières (fl. 2019) who described the first case in 1984.

Differential diagnoses

Although many other leukodystrophies are viable differential diagnoses, additional conditions to be considered include:

  • antenatal/perinatal infections (e.g. TORCH infections)
  • band-like calcification polymicrogyria (BLC-PMG; pseudo-TORCH syndrome) 
  • classic Cockayne syndrome (CS type 1)
  • cerebroretinal microangiopathy with calcifications and cysts (CRMCC; Coats plus)
  • Hoyeraal Hreidarsson syndrome
  • mitochondrial cytopathies (e.g. Leigh syndrome)