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- Aicardi–Goutières_syndrome abstract "Aicardi–Goutières syndrome (AGS) is a congenital immune-mediated neurodevelopmental disorder caused by mutations in the SAMHD1, TREX1, Ribonuclease H2 (RNASEH2A, RNASEH2B, RNASEH2C) and ADAR genes. This neurological disease usually presents at the age of four months and is characterized by the neurological symptoms of cerebral calcification (accumulation of calcium), white matter abnormalities, and cerebral atrophy. It is a type of autosomal recessive leukodystrophy, usually presenting within the first few weeks of life, and it is generally fatal within the first few years. If the patient does survive, treatment focuses on symptoms because no specific treatment has been developed to target the cause. It is also known as Cree encephalitis and pseudo-TORCH syndrome, both of which were once considered separate disorders.".
- Aicardi–Goutières_syndrome wikiPageID "38887508".
- Aicardi–Goutières_syndrome wikiPageRevisionID "605061592".
- Aicardi–Goutières_syndrome diseasesdb "31680".
- Aicardi–Goutières_syndrome genereviewsname "Aicardi–Goutières Syndrome".
- Aicardi–Goutières_syndrome genereviewsnbk "NBK1475".
- Aicardi–Goutières_syndrome icd "G31.8".
- Aicardi–Goutières_syndrome name "Aicardi–Goutières syndrome".
- Aicardi–Goutières_syndrome omim "225750".
- Aicardi–Goutières_syndrome subject Category:Genetics.
- Aicardi–Goutières_syndrome subject AIDS.
- Aicardi–Goutières_syndrome subject Category:Syndromes.
- Aicardi–Goutières_syndrome type Disease.
- Aicardi–Goutières_syndrome type Situation.
- Aicardi–Goutières_syndrome comment "Aicardi–Goutières syndrome (AGS) is a congenital immune-mediated neurodevelopmental disorder caused by mutations in the SAMHD1, TREX1, Ribonuclease H2 (RNASEH2A, RNASEH2B, RNASEH2C) and ADAR genes. This neurological disease usually presents at the age of four months and is characterized by the neurological symptoms of cerebral calcification (accumulation of calcium), white matter abnormalities, and cerebral atrophy.".
- Aicardi–Goutières_syndrome label "Aicardi-Goutières-Syndrom".
- Aicardi–Goutières_syndrome label "Aicardi–Goutières syndrome".
- Aicardi–Goutières_syndrome label "Syndrome d'Aicardi-Goutières".
- Aicardi–Goutières_syndrome label "Syndroom van Aicardi-Goutières".
- Aicardi–Goutières_syndrome label "Síndrome de Aicardi-Goutières".
- Aicardi–Goutières_syndrome label "Zespół Aicardiego-Goutièresa".
- Aicardi–Goutières_syndrome sameAs Aicardi%E2%80%93Gouti%C3%A8res_syndrome.
- Aicardi–Goutières_syndrome sameAs Aicardi-Goutières-Syndrom.
- Aicardi–Goutières_syndrome sameAs Síndrome_de_Aicardi-Goutières.
- Aicardi–Goutières_syndrome sameAs Syndrome_d'Aicardi-Goutières.
- Aicardi–Goutières_syndrome sameAs Syndroom_van_Aicardi-Goutières.
- Aicardi–Goutières_syndrome sameAs Zespół_Aicardiego-Goutièresa.
- Aicardi–Goutières_syndrome sameAs Q403453.
- Aicardi–Goutières_syndrome sameAs Q403453.
- Aicardi–Goutières_syndrome wasDerivedFrom Aicardi–Goutières_syndrome?oldid=605061592.