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Nume Polymicrogyria
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Boli A-Z Aarskog-Scott Syndrome Absence of Septum Pellucidum Adams-Oliver Syndrome Aging Al-Gazali-Bakalinova Syndrome Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity Al-Raqad Syndrome Aniridia 1 Anorexia Nervosa 1 Arachnoid Cysts Arachnoiditis Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Attention Deficit-Hyperactivity Disorder Band Heterotopia Baraitser-Winter Syndrome Bernard-Soulier Syndrome Bilateral Frontal Polymicrogyria Bilateral Generalized Polymicrogyria Bilateral Polymicrogyria Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, I System Cataract Cerebellar Hypoplasia Cerebritis Chorioretinitis Chromosomal Triplication Cohen Syndrome Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Cortical Dysplasia, Complex, with Other Brain Malformations 7 Cortical Dysplasia, Complex, with Other Brain Malformations 8 Craniosynostosis Cutis Laxa Cutis Verticis Gyrata Cutis Verticis Gyrata Mental Deficiency Dermatomyositis Ehlers-Danlos Syndrome Encephalocele Epilepsy Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation Fetal Akinesia Deformation Sequence Fetal Alcohol Syndrome Focal Dermal Hypoplasia Foix Chavany Marie Syndrome Glycogen Storage Disease Iii Hemimegalencephaly Hemiplegia Hepatic Adenomas, Familial Holoprosencephaly Hydranencephaly Hydrocephalus Hypoglycemia Hypomelanosis of Ito Knobloch Syndrome Landau-Kleffner Syndrome Lateral Sclerosis Left Ventricular Noncompaction Lennox-Gastaut Syndrome Leukodystrophy Lipomatosis Lissencephaly Macrocephaly/megalencephaly Syndrome, Autosomal Recessive Megalencephaly Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 1 Microcephaly Microtia Mowat-Wilson Syndrome Multiple Mitochondrial Dysfunctions Syndrome 5 Muscular Dystrophy Neurofibromatosis, Type Iv, of Riccardi Neuronal Migration Disorders Neuronitis Neuropathy Occipital Encephalocele Oliver Syndrome Optic Nerve Hypoplasia, Bilateral Pachygyria Periventricular Nodular Heterotopia Pituitary Hormone Deficiency, Combined, 2 Polydactyly Polymicrogyria, Bilateral Frontoparietal Polymicrogyria, Bilateral Perisylvian, Autosomal Recessive Polymicrogyria, Bilateral Perisylvian, X-Linked Polymicrogyria, Bilateral Temporooccipital Porencephaly Pseudo-Torch Syndrome 1 Retinal Detachment Retinitis Schizencephaly Scott Syndrome Spasticity Status Epilepticus Thrombocytopenia Thrombosis Tuberous Sclerosis Turner Syndrome Twin-to-Twin Transfusion Syndrome Unilateral Focal Polymicrogyria Unilateral Polymicrogyria Velocardiofacial Syndrome