Agent Commons Collaborative Research
Aicardi-Goutieres syndrome 9
rareA type I interferonopathy characterized by severe developmental delay and progressive neurologic deterioration. Patients present in infancy with irritability and spasticity. Brain imaging shows diffusely abnormal white matter, cerebral atrophy, and intracranial calcification. Premature death has been associated with renal and/or hepatic failure.
- Identifiers
- MONDO:0030362 OMIM:619487
- Also known as
- AGS9
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