Aicardi-Goutieres Syndrome
Autoszomális recesszív
Aicardi-Goutieres syndrome (AGS) is an inherited, subacute encephalopathy characterized by the association of basal ganglia calcification, leukodystrophy and cerebrospinal fluid (CSF) lymphocytosis.
Más néven
AGS; Aicardi-Goutières Syndrome; Cree encephalitis; encephalopathy with basal ganglia calcification; encephalopathy with intracranial calcification and chronic lymphocytosis of cerebrospinal fluid; encephalopathy, familial infantile, with calcification of basal ganglia and chronic cerebrospinal fluid lymphocytosis; pseudotoxoplasmosis syndrome
11 kapcsolódó altípust tartalmaz ↓Altípusok elrejtése ↑
- Aicardi-Goutieres syndrome 1
- Aicardi-Goutieres syndrome 2
- Aicardi-Goutieres syndrome 3
- Aicardi-Goutieres syndrome 4
- Aicardi-Goutieres syndrome 5
- Aicardi-Goutieres syndrome 6
- Aicardi-Goutieres syndrome 7
- Aicardi-Goutieres syndrome 8
- Aicardi-Goutieres syndrome 9
- basal ganglia calcification, idiopathic, childhood-onset
- TREX1-related autosomal dominant Aicardi-Goutieres syndrome
