Aicardi–Goutières syndrome
Aicardi–Goutières syndrome (AGS), which is completely distinct from the similarly named Aicardi syndrome, is a rare, usually early onset childhood, inflammatory disorder most typically affecting the brain and the skin (neurodevelopmental disorder). The majority of affected individuals experience significant intellectual and physical problems, although this is not always the case. The clinical features of AGS can mimic those of in utero acquired infection, and some characteristics of the condition also overlap with the autoimmune disease systemic lupus erythematosus (SLE). Following an original description of eight cases in 1984, the condition was first referred to as 'Aicardi–Goutières syndrome' (AGS) in 1992, and the first international meeting on AGS was held in Pavia, Italy, in 2001.
primaryTopic
Aicardi–Goutières syndrome
Aicardi–Goutières syndrome (AGS), which is completely distinct from the similarly named Aicardi syndrome, is a rare, usually early onset childhood, inflammatory disorder most typically affecting the brain and the skin (neurodevelopmental disorder). The majority of affected individuals experience significant intellectual and physical problems, although this is not always the case. The clinical features of AGS can mimic those of in utero acquired infection, and some characteristics of the condition also overlap with the autoimmune disease systemic lupus erythematosus (SLE). Following an original description of eight cases in 1984, the condition was first referred to as 'Aicardi–Goutières syndrome' (AGS) in 1992, and the first international meeting on AGS was held in Pavia, Italy, in 2001.
has abstract
Aicardi-Goutières Syndrom (AGS ...... dert Fälle beschrieben worden.
@de
Aicardi–Goutières syndrome (AG ...... st 400 cases of AGS are known.
@en
El síndrome de Aicardi-Goutièr ...... to efectivo contra sus causas.
@es
Het syndroom van Aicardi-Gouti ...... reguliere fondsen beschikbaar.
@nl
Le syndrome d’Aicardi-Goutière ...... icardi et Françoise Goutières.
@fr
Zespół Aicardiego-Goutièresa, ...... yło ich prawdopodobnie więcej.
@pl
ICD10
OMIM id
Wikipage page ID
38,887,508
Wikipage revision ID
743,204,423
DiseasesDB
GeneReviewsName
Aicardi–Goutières Syndrome
GeneReviewsNBK
Orphanet
comment
Aicardi-Goutières Syndrom (AGS ...... dert Fälle beschrieben worden.
@de
Aicardi–Goutières syndrome (AG ...... held in Pavia, Italy, in 2001.
@en
El síndrome de Aicardi-Goutièr ...... to efectivo contra sus causas.
@es
Het syndroom van Aicardi-Gouti ...... reguliere fondsen beschikbaar.
@nl
Le syndrome d’Aicardi-Goutière ...... icardi et Françoise Goutières.
@fr
Zespół Aicardiego-Goutièresa, ...... yło ich prawdopodobnie więcej.
@pl
label
Aicardi-Goutières-Syndrom
@de
Aicardi–Goutières syndrome
@en
Syndrome d'Aicardi-Goutières
@fr
Syndroom van Aicardi-Goutières
@nl
Síndrome de Aicardi-Goutières
@es
Zespół Aicardiego-Goutièresa
@pl
sameAs
wasDerivedFrom
isPrimaryTopicOf
name
Aicardi–Goutières syndrome
@en