Child Neurology Foundation
601 W. Short Street
Lexington, KY, USA
888-417-3435
About Child Neurology Foundation
The Child Neurology Foundation (CNF) connects partners from all areas of the child neurology community so those navigating the journey of disease diagnosis, management, and care have the ongoing support from those dedicated to treatments and cures. Our expanding network of patients and caregivers, volunteers and advocates, researchers and clinicians is committed to helping one another along the path that leads to the best quality of care — and the highest quality of life—for every child. CNF’s mission is to serve as a collaborative center of education, resources, and support for children and their families living with neurologic conditions, and facilitate connection with medical professionals who care for them.
Related Rare Diseases:
- STXBP1 Disorders
- Arginine: Glycine Amidinotransferase Deficiency
- Guanidinoacetate Methyltransferase Deficiency
- Creatine Transporter Deficiency
- Kufor Rakeb Syndrome
- SETBP1 Haploinsufficiency Disorder
- KAT6A Syndrome
- Cerebral Creatine Deficiency Syndromes
- Pitt-Hopkins Syndrome
- Febrile Infection-Related Epilepsy Syndrome (FIRES)
- NORSE (New Onset Refractory Status Epilepticus) and FIRES (Febrile Infection-Related Epilepsy Syndrome)
- MECP2 Duplication Syndrome
- Congenital Muscular Dystrophy
- Distal Myopathy
- Spinal Muscular Atrophy
- West Syndrome
- Cerebellar Agenesis
- Limb-Girdle Muscular Dystrophies
- Giant Axonal Neuropathy
- Emery Dreifuss Muscular Dystrophy
- Myotonia Congenita
- Myotonic Dystrophy
- Charcot-Marie-Tooth Disease
- Rett Syndrome
- Cerebral Palsy
- Status Epilepticus
- Duchenne Muscular Dystrophy
- Werdnig-Hoffmann Disease
- Dystonia
- Multiple Sclerosis
- Friedreich’s Ataxia
- Tourette Syndrome
- KAT6B-Related Disorders
- CTNNB1 Syndrome
- Landau Kleffner Syndrome
- Síndrome CTNNB1
- Síndrome de anomalías congénitas múltiples asociado al gen KAT6B
- Distrofia muscular de Duchenne
- Atrofia muscular espinal
- Deficiencia de L-arginina:glicina amidinotransferasa
- Agenesia cerebelar
- Síndrome KAT6A
- Deficiencia de guanidinoacetato metiltransferasa
- Molybdenum Cofactor Deficiency
- Deficiencia de cofactor de molibdeno
