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Nume Focal Epilepsy
Pagina Web www.malacards.org
Clasificare anatomică Malacards Boli neuronale

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Boli A-Z 47, Xxy Adolescence-Adult Electroclinical Syndrome Adult-Onset Still's Disease Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Alzheimer Disease 3 Amnestic Disorder Anauxetic Dysplasia 1 Aneurysm Angiomatosis Angiomyolipoma Aniridia 1 Anorexia Nervosa 1 Aortic Disease Aphasia Arachnoid Cysts Arachnoiditis Arthrochalasia Ehlers-Danlos Syndrome Asplenia, Isolated Congenital Ataxia and Polyneuropathy, Adult-Onset Attention Deficit-Hyperactivity Disorder Audiogenic Seizures Autoimmune Encephalitis Autosomal Dominant Epilepsy with Auditory Features Autosomal Dominant Nocturnal Frontal Lobe Epilepsy Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 2 Ayme-Gripp Syndrome Benign Ependymoma Benign Epilepsy with Centrotemporal Spikes Benign Infantile Focal Epilepsy with Midline Spikes and Wave During Sleep Blood Group--Ahonen Blood Group, I System Bone Cancer Burning Mouth Syndrome Cardiac Arrhythmia Cdkl5-Related Disorder Central Nervous System Disease Cerebritis Childhood Absence Epilepsy Childhood Electroclinical Syndrome Chorioamnionitis Chromosomal Triplication Chromosome Xq Deletion Corneal Dystrophy, Fleck Cortical Dysplasia, Complex, with Other Brain Malformations 7 Coumarin Resistance Dysautonomia Dysembryoplastic Neuroepithelial Tumor Dystonia Early Myoclonic Encephalopathy Encephalitis Encephalocele Encephalopathy Epilepsy Epilepsy, Familial Focal, with Variable Foci 1 Epilepsy, Idiopathic Generalized Epilepsy, Idiopathic Generalized 10 Epilepsy, Idiopathic Generalized 7 Epilepsy, Nocturnal Frontal Lobe, 1 Epilepsy, Nocturnal Frontal Lobe, 3 Epilepsy, Reading Epilepsy with Generalized Tonic-Clonic Seizures Epileptic Encephalopathy, Early Infantile, 15 Epileptic Encephalopathy, Early Infantile, 6 Febrile Seizures Febrile Seizures, Familial, 11 Female Reproductive System Disease Focal Cortical Dysplasia, Type Ii Focal Dystonia Fragile X Syndrome Galactose Epimerase Deficiency Generalized Epilepsy with Febrile Seizures Plus Glioma Haim-Munk Syndrome Headache Hemifacial Atrophy, Progressive Hemiplegia Hepatic Adenomas, Familial Hepatitis Hyperglycemia Hypochondroplasia Hypoparathyroidism Infancy Electroclinical Syndrome Infantile Epileptic Encephalopathy Intracranial Aneurysm Ischemia Joint Disorders Juvenile Rheumatoid Arthritis Kidney Angiomyolipoma Kidney Benign Neoplasm Lacrimal Apparatus Disease Landau-Kleffner Syndrome Lennox-Gastaut Syndrome Lung Disease Lymphangioleiomyomatosis Malignant Migrating Partial Seizures of Infancy Meningitis Myoclonic Astatic Epilepsy Myoclonic Epilepsy of Infancy Myoclonus Myotonic Dystrophy Neurodegeneration with Brain Iron Accumulation 2a Neuronitis Periodic Limb Movement Disorder Pitt-Hopkins Syndrome Porphyria Primary Familial Brain Calcification Prostatic Adenoma Pseudohypoparathyroidism Psychotic Disorder Pulmonary Alveolar Microlithiasis Pulpitis Recurrent Corneal Erosion Reproductive System Disease Seizure Disorder Seizures, Benign Familial Infantile, 3 Spinal Meningioma Spinocerebellar Ataxia 6 Spiradenoma Status Epilepticus Subependymal Giant Cell Astrocytoma Subependymal Glioma Temporal Lobe Epilepsy Tetanus Toxic Encephalopathy Treacher Collins Syndrome 1 Tremor Tuberous Sclerosis Tuberous Sclerosis 1 Tuberous Sclerosis 2 West Syndrome