Table 1.
Group of diseases | Diseases | Diagnostic test | |
---|---|---|---|
Inherited | Malformation | Dandy-Walker malformation | Brain MRI findings |
Joubert syndrome | Brain MRI findings | ||
Rhombencephalosynapsis | Brain MRI findings | ||
Pontocerebellar hypoplasias | Brain MRI findings, genetic analysis | ||
Congenital muscular dystrophy due to α-dystroglycanopathy | Muscle biopsy, genetic analysis | ||
Brainstem disconnection | Brain MRI findings | ||
Pontine tegmental cap dysplasia | Brain MRI findings | ||
Chiari type II malformation | Brain MRI findings | ||
Neurometabolic | Congenital disorders of glycosylation | Transferrin electrophoresis, genetic analysis | |
Smith-Lemli-Opitz syndrome | Elevated 7-dehydrocholesterol, genetic analysis | ||
Non-ketotic hyperglycinemia | Elevated CSF glycine concentration and CSF-to-plasma glycine ratio, genetic analysis | ||
Maple syrup urine disease | Elevated branched-chain amino acids and branched-chain keto-acids in blood and urine | ||
Pyruvate dehydrogenase deficiency | Abnormal enzyme function, genetic analysis | ||
Sulfite oxidase deficiency | Elevated sulfite, thiosulfate, taurine, and S-sulfocysteine concentrations in urine, genetic analysis | ||
Neurodegenerative | Krabbe disease | Low galactocerebrosidase activity in peripheral leukocytes, genetic analysis | |
Cockayne syndrome | Genetic analysis | ||
Pelizaeus-Merzbacher disease | Genetic analysis | ||
Aicardi-Goutières syndrome | Genetic analysis | ||
Congenital neuronal ceroid lipofuscinosis | Genetic analysis | ||
Spinocerebellar ataxias | SCA type 2 | Genetic analysis | |
SCA type 7 | Genetic analysis | ||
Acquired | Vascular | Cerebellar hemorrhage | Brain MRI findings |
Sinovenous thrombosis | Brain MRI findings | ||
cerebellar ischemic stroke | Brain MRI findings | ||
Disrupted development of the cerebellum in preterms | History of prematurity, brain MRI findings | ||
Hypoxic-ischemic injury | Brain MRI findings | ||
Infection | Congenital cytomegalovirus | Viral culture, PCR, or serology within the first weeks of life, later PCR for CMV DNA in dried blood of neonatal screening | |
Herpes simplex | CSF viral culture or PCR | ||
Toxic | Glucocorticoids | Brain MRI findings, history of glucocorticoids therapy | |
Teratogens | Alcohol | History, brain MRI findings | |
Retinoic acid | History, brain MRI findings | ||
Misoprostol | History, brain MRI findings | ||
Tumors | Teratoma | Histology | |
Medulloblastoma | Histology |
CMV cytomegalovirus, CSF cerebrospinal fluid, DNA deoxyribonucleic acid, MRI magnetic resonance imaging, PCR polymerase chain reaction