Target Individuals

• Individuals presenting with the most common symptoms of a neurological disease

• Individuals with a positive family history of neurological disease

• Individuals without a positive family history but with symptoms resembling the specific disease indication

• Individuals with a negative, but suspected, family history, in order to perform genetic counseling (prenatal analyses are recommended in families of affected individuals)

Inherited Neuro-developmental disorders multigene NGS Panels

Test NameTest DetailsCurrency Add To Cart
FM-NU-001Epilepsy- Myoclonic Epilepsy, Generalized Epilepsy, Infantile Epilepsy, Temporal Lobe Epilepsy, Focal Epilepsy, Neuronal Ceroid Lipofuscinosis, Generalized epilepsy with febrile seizures plus, Intellectual disability-asscociated epilepsy and other related conditions.

42,000.00 Add to cart

FM-NU-002MicroCephaly- Primary microcephaly, Aicardi-Goutieres Syndrome, Coffin-Siris Syndrome, Seckel Syndrome, Meier-Gorlin Syndrome, Angelman Syndrome, Cornelia de Lange Syndrome,Intellectual disability-asscociated microcephaly and other related conditions.

42,000.00 Add to cart

FM-NU-003Macrocephaly- Cardiofaciocutaneous Syndrome, Mucopolysaccharidosis, Megalencephaly and other related conditions.

42,000.00 Add to cart

FM-NU-004Congenital Brain Malformations- Joubert Syndrome, Lissencephaly, Meckel Syndrome, Polymicrogyria, Muscular Dystrophy-dytroglycanopathy, Pontocerebellar Hypoplasia, Aicardia-Goutieres Syndrome, HoloProsencephalyand other related conditions.

42,000.00 Add to cart

Inherited Neuro-Muscular Disorders multigene NGS Panels

Test NameTest DetailsCurrencyAdd To Cart
FM-NU-005Muscular Dystrophy- Collagen Type VI-related Disorders, Dystroglycanopathy, Dystrophinopathy, Emery-Dreifuss muscular Dystrophy, Limb-girdle muscular dystrophy and others.

42,000.00 Add to cart

FM-NU-006Dystonia- Focan and generalized dystonia, Complex dystonia, Parkinsonism associated Dystonia and others.

42,000.00 Add to cart

FM-NU-007Ataxia- Cerebellar Ataxia, Spinocerebellar Ataxia, Episodic Ataxia, Spastic Paraplegia associated Ataxia, Neuronal Ceroid lipofuscinosis, Mitchondrial Disorders associated Ataxia, Epilepsy associated Ataxia.

42,000.00 Add to cart

FM-NU-008Congenital Myopathy- Nemaline Myopathy, Distal Myopathy, Myofibrillar Myopathy, Centronuclear myopathy, Bethlem myopathy, Congenital fiber-type disproportion and others.

42,000.00 Add to cart

FM-NU-009Spastic Paraplegia.

42,000.00 Add to cart

FM-NU-010Neuropathy- Hereditary motor and sensory neuropathy, Charcot-Marie-Tooth disease, Peripheral Neuropathy, Axonal Neuropathy, Dejerine-sottas disease,Polyneuropathy, Amyloidosis associated neuropathy, Ataxia associated neuropathy and others.

42,000.00 Add to cart

Neurology PGx Tests

Test NameTest DetailsCurrencyAdd To Cart
FM-NUPGx-011Carbamazepine Sensitivity - based on HLA-B Genotyping.

6,000.00 Add to cart

FM-NUPGx-012Divalproex sodium and Valproic Acid- POLG gene mutation detection for use of Divalproex sodium (contraindicated in NeuroMetabolic Syndromes.)

6,000.00 Add to cart

FM-NUPGx-013Clobazam Dosage- Individual metabolizer Status and dosage based CYP2C19 genotyping.

6,000.00 Add to cart

FM-NUPGx-014NeuroPGx mini Panel test- Drug response and dosages for use of Anti-Platelets

6,000.00 Add to cart