Registered cases


Registered cases

Gender distribution
Gender Count
Male 5
Female 3
Diet type distribution
Diet Type Count
classic 3
LGIT 0
ATKINS 1
# Diagnose names Count
1Acquired epileptic aphasia (Landau-Kleffner Syndrome)0
2Adenylosuccinate lyase (ADSL) deficiency0
3Associated with Leigh’s syndrome0
4Autism 0
5Glucose transporter protein 1 (GLUT-1) deficiency0
6Glycogenosis type V (McArdle disease)0
7Infantile spasms0
8Ketotic hypoglycemia0
9Lafora body disease0
10Mitochondrial respiratory chain complex defects0
11Myoclonic-astatic epilepsy (Doose syndrome)0
12Phosphofructokinase deficiency0
13Pyruvate dehydrogenase deficiency (PDHD)0
14Refractory Seizure0
15Severe myoclonic epilepsy of infancy (Dravet syndrome)0
16Subacute Sclerosing Panencephalitis (SSPE)0
17Succinic semialdehyde dehydrogenase (SSADH Deficiency)0