Aicardi-Goutieres syndrome 8
MONDO:0030361A type I interferonopathy characterized by severe developmental delay and progressive neurologic deterioration ending in premature death. Brain imaging shows diffusely abnormal white matter, severe cerebral atrophy, and intracranial calcification.
Also known as: AGS8, Aicardi-Goutieres syndrome 8
52 clinical trials for this condition and its sub-types, 0 tagged with Aicardi-Goutieres syndrome 8 itself.
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