ORDERTest Kits
METHOD KEY
- Sequencing with CNVPGxome
- Sequencing with CNVPG-Select
- CNV via aCGH
- Sanger Sequencing
- MLPA
- Repeat Expansion
- Other
Neurologic Disorders
Our comprehensive neurology genetic test menu offers genetic tests and panels for various neurologic disorders and has been meticulously curated by our expert PhD team. PreventionGenetics offers genetic testing for various neurologic conditions such as Autism Spectrum Disorders (ASD), Alzheimer’s, epilepsy and much more. Accurate genetic testing is imperative for diagnosis, informed treatment decisions and identifying other family members who may be at risk.
Acyl-CoA Dehydrogenase Deficiency
Agnathia-Otocephaly Complex
Aicardi-Goutieres Syndrome
Alzheimer's Disease
Amyloidosis
Amyotrophic Lateral Sclerosis (ALS)
Ataxia
Ataxia-Oculomotor Apraxia
Autism Spectrum Disorders
BBB Syndrome
Benign familial infantile epilepsy
Brain Malformations
Brown-Vialetto-Van Laere Syndrome
CADASIL
CADASIL and CARASIL
CHARGE Syndrome
Cerebral Cavernous Malformations
Cerebral Small Vessel Diseases
Ceroid Lipofuscinoses
Charcot Marie Tooth
Chromosomal Instability Syndromes
Congenital Central Hypoventilation syndrome
Congenital Myopathy
Copper Metabolism Disorders
Dementia
Dentatorubral-Pallidoluysian Atrophy (DRPLA)
Developmental Delay
Distal Hereditary Myopathy
Dystonia
Dystrophinopathies
Epilepsy
Fazio-Londe Disease
Fragile X Syndrome
Frontotemporal Dementia
Galloway-Mowat Syndrome
Glutaric Acidemia
Greig Cephalopolysyndactyly Syndrome
Hemiplegic Migraine
Hirschsprung Disease
Holoprosencephaly
Huntington Disease
Hydrocephalus
Hyperammonemia
Hypoglycemia
Intellectual Disability
Joubert Syndrome
Kallmann Syndrome
L1 Syndrome
Leukodystrophy
Leukoencephalopathy
Lissencephaly
Lysosomal Storage Disorders
Macrocephaly
Methylmalonic Acidemia
Microcephaly
Mitochondrial Disorders
Movement Disorders
Muscular Dystrophy
Neuroaxonal Dystrophy
Neurodegeneration
Neurofibromatosis
Neuropathy
Opitz G
Organic Acidurias
Osteodysplasia
Pallister-Hall Syndrome
Parkinson Disease
Peroxisomal Disorders
Pontocerebellar Hypoplasia
Porphyria
Premature Ovarian Failure (POF1)
Rasopathies
Rett Syndrome
Rett Syndrome, Angelman Syndrome and Variant Syndromes
Schwannomatosis
Septo-optic Dysplasia
Spastic Paraplegia
Stroke, Cerebral Hemorrhage, Hemiplegia and Migraines
Stuttering
Tay-Sachs Disease (GM2 Gangliosidosis Type 1)
Tuberous Sclerosis
Warburg Micro Syndrome
Wolfram Syndrome
METHOD KEY
- Sequencing with CNVPGxome
- Sequencing with CNVPG-Select
- CNV via aCGH
- Sanger Sequencing
- MLPA
- Repeat Expansion
- Other