Informaţii despre

Nume West Syndrome
Pagina Web www.malacards.org
Clasificare globală Malacards Boli rare
Clasificari ICD10 Other generalized epilepsy and epileptic syndromes
Clasificare anatomică Malacards Boli neuronale

Vezi şi

Boli A-Z Acth Deficiency, Isolated Aging Aicardi Syndrome Alacrima, Achalasia, and Mental Retardation Syndrome Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Androgen Insensitivity Syndrome, Mild Aniridia 1 Anorexia Nervosa 1 Aortic Valve Disease 2 Arachnoiditis Arthrochalasia Ehlers-Danlos Syndrome Autism Autonomic Dysfunction Axonal Neuropathy Basal Cell Carcinoma Behr Syndrome Benign Familial Infantile Epilepsy Benign Familial Neonatal Epilepsy Benign Neonatal Seizures Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Brain Injury Cdkl5-Related Disorder Cerebral Hemorrhage Cerebritis Childhood Absence Epilepsy Childhood Electroclinical Syndrome Christianson Syndrome Chromosomal Triplication Chromosome 7q Duplication Chromosome 8p Duplication Chromosome 9p Deletion Syndrome Chronic Meningitis Congenital Toxoplasmosis Crouzon Syndrome with Acanthosis Nigricans D-Glyceric Aciduria Diabetes and Deafness, Maternally Inherited Diabetes Mellitus Down Syndrome Dystonia Early Myoclonic Encephalopathy Encephalopathy Epilepsy Epilepsy, Nocturnal Frontal Lobe, 1 Epilepsy with Generalized Tonic-Clonic Seizures Epileptic Encephalopathy, Early Infantile, 1 Epileptic Encephalopathy, Early Infantile, 14 Epileptic Encephalopathy, Early Infantile, 15 Epileptic Encephalopathy, Early Infantile, 3 Epileptic Encephalopathy, Early Infantile, 4 Epileptic Encephalopathy, Early Infantile, 6 Epileptic Encephalopathy, Early Infantile, 7 Epileptic Encephalopathy, Early Infantile, 9 Focal Epilepsy Gastroenteritis Generalized Epilepsy with Febrile Seizures Plus Hemophilia Hemophilia a Holoprosencephaly Hydrocephalus Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperinsulinemic Hypoglycemia Hyperlexia Hypoglycemia Hypomelanosis of Ito Hypophosphatasia Hypotonia Infancy Electroclinical Syndrome Infantile Epileptic Encephalopathy Kabuki Syndrome 1 Landau-Kleffner Syndrome Leigh Syndrome Lennox-Gastaut Syndrome Leukomalacia Lissencephaly Lutheran Suppressor, X-Linked Malignant Migrating Partial Seizures of Infancy Meningitis Mental Retardation, X-Linked, Syndromic 13 Mental Retardation, X-Linked, Syndromic, Hedera Type Microcephaly Monocarboxylate Transporter 1 Deficiency Mood Disorder Muscular Dystrophy Muscular Dystrophy, Duchenne Type Myoclonic Astatic Epilepsy Myoclonic Epilepsy of Infancy Neonatal Hypoxic and Ischemic Brain Injury Neonatal Period Electroclinical Syndrome Neurofibromatosis, Type Iv, of Riccardi Neuronal Migration Disorders Neuronitis Neuropathy Opiate Dependence Pallister-Killian Mosaic Syndrome Pallister-Killian Syndrome Panic Disorder Paraphimosis Partington X-Linked Mental Retardation Syndrome Periventricular Leukomalacia Periventricular Nodular Heterotopia Phelan-Mcdermid Syndrome Phenylketonuria Phosphoglycerate Dehydrogenase Deficiency Porencephaly Premenstrual Tension Pyruvate Dehydrogenase E1-Alpha Deficiency Quadriplegia Rett Syndrome Reye Syndrome Riddle Syndrome Schinzel Giedion Syndrome Seizure Disorder Seizures, Benign Familial Infantile, 3 Senile Entropion Severe Combined Immunodeficiency Severe Hemophilia a Skin Tag Smith-Magenis Syndrome Sotos Syndrome 1 Spasticity Spastic Quadriplegia Status Epilepticus Temporal Lobe Epilepsy Thyroid Crisis Toxoplasmoză Tuberous Sclerosis Undetermined Early-Onset Epileptic Encephalopathy Undifferentiated Pleomorphic Sarcoma Visual Epilepsy Vitamin B12 Deficiency Wolf-Hirschhorn Syndrome X-Linked Non-Specific Intellectual Disability