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Nume Status Epilepticus
Pagina Web
Clasificare globală Malacards Cancer diseases; Rare diseases
Clasificari ICD10 Grand mal status epilepticus; S
Clasificare anatomică Malacards Neuronal diseases

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Boli A-Z 3-Methylcrotonyl-Coa Carboxylase Deficiency Acute Encephalopathy with Biphasic Seizures and Late Reduced Diffusion Acute Respiratory Distress Syndrome Adjustment Disorder Aging Agraphia Alexia Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Alport Syndrome, X-Linked Al-Raqad Syndrome Amnestic Disorder Aneurysm Angelman Syndrome Aniridia 1 Anorexia Nervosa 1 Anoxia Antiphospholipid Syndrome Aphasia Arachnoid Cysts Arachnoiditis Argininemia Arthrochalasia Ehlers-Danlos Syndrome Astroblastoma Audiogenic Seizures Autism Autoimmune Encephalitis Autonomic Nervous System Neoplasm Axonal Neuropathy Bacterial Meningitis Barbiturate Abuse Benign Adult Familial Myoclonic Epilepsy Benign Childhood Occipital Epilepsy, Panayiotopoulos Type Beta-Adrenergic Stimulation, Response to Beta-Ureidopropionase Deficiency Bipolar Disorder Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Brain Edema Brain Injury Breast Cancer Breast Fibrosarcoma Brugada Syndrome Capgras Syndrome Capillary Leak Syndrome Carcinoid Syndrome Cardiac Arrest Carotid Stenosis Cat-Scratch Disease Cavernous Hemangioma Central Cord Syndrome Central Nervous System Disease Central Neurocytoma Cerebellar Medulloblastoma Cerebral Atrophy Cerebral Folate Deficiency Cerebritis Christianson Syndrome Chromosome 9p Duplication Coffin-Lowry Syndrome Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Cortical Blindness Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome Craniosynostosis with Fibular Aplasia Creutzfeldt-Jakob Disease Cysticercosis Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome Dentatorubral-Pallidoluysian Atrophy Duodenal Somatostatinoma Dysgerminoma of Ovary Echolalia Efavirenz, Poor Metabolism of Encephalitis Encephalopathy Endocarditis Endotheliitis Ependymoma Epilepsy Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation Epileptic Encephalopathy, Early Infantile, 6 Familial Hemiplegic Migraine Fanconi Syndrome Febrile Infection-Related Epilepsy Syndrome Febrile Seizures Fetal Alcohol Spectrum Disorder Fetal Alcohol Syndrome Focal Epilepsy Fragile X Syndrome Fryns Syndrome Galactorrhea Ganglioglioma Ganglioneuroblastoma Ganglioneuroma Glioma Griscelli Syndrome Hashimoto's Encephalitis Headache Helix Syndrome Hemangioma Hemimegalencephaly Hemiplegic Migraine Hemometra Hemophagocytic Lymphohistiocytosis Hepatic Adenomas, Familial Hepatic Encephalopathy Hepatitis Herpes Simplex Herpes Simplex Encephalitis Hhv-6 Encephalitis Holoprosencephaly Huntington Disease Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperekplexia Hyperglycemia Hypersomnia Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertensive Encephalopathy Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypoglycemia Hypoparathyroidism Hypoxia Idiopathic Recurrent Stupor Incontinentia Pigmenti Influenza Intracranial Cysts Intracranial Hypotension Isoniazid Toxicity Jeavons Syndrome Kluver-Bucy Syndrome L-2-Hydroxyglutaric Aciduria Lactic Acidosis Landau-Kleffner Syndrome Large Cell Carcinoma with Rhabdoid Phenotype Lennox-Gastaut Syndrome Limbic Encephalitis Lupus Erythematosus Lymphoma Malaria, Mild Malignant Migrating Partial Seizures of Infancy Malignant Spiradenoma Maple Syrup Urine Disease Meckel Syndrome, Type 1 Melanotic Medulloblastoma Melanotic Neuroectodermal Tumor Meningitis Meningoencephalitis Metabolic Acidosis Mitochondrial Dna Depletion Syndrome 4a Mitochondrial Myopathy Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes Mixed Ductal-Endocrine Carcinoma Mowat-Wilson Syndrome Mucopolysaccharidosis-Plus Syndrome Mucopolysaccharidosis, Type Ii Multiple Sclerosis Mungan Syndrome Muscular Atrophy Mutism Myocardial Stunning Myoclonic Astatic Epilepsy Myoclonus Myoclonus Epilepsy Myopathy Neonatal Hypoxic and Ischemic Brain Injury Neuraminidase Deficiency Neurenteric Cyst Neuroleptic Malignant Syndrome Neuronal Ceroid-Lipofuscinoses Neuronitis Neuropathy Neurosarcoidosis Neurosyphilis Niemann-Pick Disease, Type a Nodular Ganglioneuroblastoma Norse Ocular Motor Apraxia Oligodendroglioma Osteogenic Sarcoma Pancreatic Somatostatinoma Paragonimiasis Peripheral Nervous System Neoplasm Pituitary Apoplexy Pneumococcal Meningitis Pneumonia Polyhydramnios Polymicrogyria Porphyria Porphyria Variegata Primary Angiitis of the Central Nervous System Primitive Neuroectodermal Tumor of the Cervix Uteri Progressive Multifocal Leukoencephalopathy Progressive Myoclonus Epilepsy Prosopagnosia Psoriasis 2 Psoriasis 7 Pulmonary Edema Purpura Pyridoxine Deficiency Quadriplegia Rasmussen Encephalitis Recurrent Hypersomnia Retrograde Amnesia Retroperitoneal Neuroblastoma Rheumatic Heart Disease Ring Chromosome 14 Syndrome Ring Chromosome 20 Rubella Sakati Syndrome Schizencephaly Schizophrenia Scrub Typhus Shigellosis Somatostatinoma Sparganosis Spina Bifida Occulta Spinal Cord Injury Spinal Muscular Atrophy Spinal Muscular Atrophy with Progressive Myoclonic Epilepsy Spiradenoma Split-Hand/foot Malformation 1 Spondyloocular Syndrome Spondyloperipheral Dysplasia Sturge-Weber Syndrome Subacute Bacterial Endocarditis Subclavian Steal Syndrome Substance Abuse Succinic Semialdehyde Dehydrogenase Deficiency Sveinsson Chorioretinal Atrophy Synucleinopathy Systemic Lupus Erythematosus Temporal Lobe Epilepsy Thrombosis Thrombotic Thrombocytopenic Purpura Thyroiditis Toxic Encephalopathy Traumatic Brain Injury Tuberculous Meningitis Tuberous Sclerosis Unilateral Polymicrogyria Uremia Vasculitis Vertebral Artery Occlusion Vohwinkel Syndrome, Variant Form Von Economo's Disease Weber Syndrome West Nile Encephalitis West Syndrome Wild Type Attr Amyloidosis Wolf-Hirschhorn Syndrome