Informaţii despre

Nume Leukodystrophy
Pagina Web www.malacards.org
Clasificare globală Malacards Boli rare
Clasificare anatomică Malacards Boli neuronale

Vezi şi

Boli A-Z 3-Methylcrotonyl-Coa Carboxylase Deficiency Acute Disseminated Encephalomyelitis Adrenoleukodystrophy Aging Alexander Disease Alopecia 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 Anauxetic Dysplasia 1 Androgen Insensitivity Syndrome, Mild Aniridia 1 Anorexia Nervosa 1 Argininosuccinic Aciduria Arthrochalasia Ehlers-Danlos Syndrome Aspartylglucosaminuria Ataxia and Polyneuropathy, Adult-Onset Ataxia Neuropathy Spectrum Ataxia-Oculomotor Apraxia 3 Ataxia-Telangiectasia Auditory Neuropathy Spectrum Disorder Autonomic Dysfunction Autosomal Dominant Leukodystrophy with Autonomic Disease Autosomal Recessive Sideroblastic Anemia Axonal Neuropathy Bipolar Disorder Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Brainstem Auditory Evoked Responses Branchiootic Syndrome 1 Canavan Disease Carbamoyl Phosphate Synthetase I Deficiency, Hyperammonemia Due to Cataract Cataract 5, Multiple Types Central Nervous System Disease Cerebral Arteriopathy, Autosomal Recessive, with Subcortical Infarcts and Leukoencephalopathy Cerebral Degeneration Cerebral Lipidosis Cerebritis Cerebrotendinous Xanthomatosis Childhood Ataxia with Central Nervous System Hypomyelination/vanishing White Matter Cholecystitis Cholelithiasis Communicating Hydrocephalus Conduct Disorder Cone-Rod Dystrophy 2 Congenital Cytomegalovirus Congenital Fiber-Type Disproportion Cutis Laxa Cytomegalovirus Infection Darier-White Disease Dementia Demyelinating Disease Dystonia Early-Onset Familial Alzheimer Disease Ehlers-Danlos Syndrome Ehlers-Danlos Syndrome, Periodontal Type, 1 Encephalomyopathy Endotheliitis Epilepsy Farber Lipogranulomatosis Fucosidosis Gaucher Disease, Type Iii Giant Axonal Neuropathy Graft-Versus-Host Disease Hantavirus Pulmonary Syndrome Hashimoto Thyroiditis Hematopoietic Stem Cell Transplantation Hemihyperplasia, Isolated Hurler Syndrome Hydrocephalus Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypogonadism Hypogonadotropic Hypogonadism Hypogonadotropism Hypomyelinating Leukodystrophy Hypomyelinating Leukoencephalopathy Hypomyelination with Brainstem and Spinal Cord Involvement and Leg Spasticity Ichthyosis, Congenital, Autosomal Recessive 11 Infantile Krabbe Disease Infertility Influenza Kearns-Sayre Syndrome Krabbe Disease Learning Disability Leigh Syndrome Leukodystrophy, Hypomyelinating, 2 Leukodystrophy, Hypomyelinating, 4 Leukodystrophy, Hypomyelinating, 5 Leukodystrophy, Hypomyelinating, 6 Leukoencephalopathy, Hereditary Diffuse, with Spheroids Leukoencephalopathy with Vanishing White Matter Lipid Storage Disease Lissencephaly Lysosomal Storage Disease Macrocephaly/megalencephaly Syndrome, Autosomal Recessive Mannosidosis Medulloblastoma Megalencephalic Leukoencephalopathy with Subcortical Cysts 1 Megalencephaly Menkes Disease Metabolic Acidosis Metachromatic Leukodystrophy Metachromatic Leukodystrophy, Adult Form Metachromatic Leukodystrophy, Juvenile Form Metachromatic Leukodystrophy, Late Infantile Form Microcephaly Mitochondrial Complex I Deficiency Mitochondrial Complex Ii Deficiency Mitochondrial Encephalomyopathy Mucolipidosis Iv Mucopolysaccharidosis-Plus Syndrome Multiple Acyl-Coa Dehydrogenase Deficiency Multiple Sclerosis Multiple Sulfatase Deficiency Muscular Dystrophy Mutism Nervous System Disease Neurogenic Bladder Neuronitis Neuropathy Neuropathy, Hereditary Sensory and Autonomic, Type Iii Obstructive Hydrocephalus Pachygyria Pelizaeus-Merzbacher Disease Peripheral Nervous System Disease Peroxisomal Acyl-Coa Oxidase Deficiency Phelan-Mcdermid Syndrome Phosphoglycerate Kinase Deficiency Pol Iii-Related Leukodystrophies Polr3-Related Leukodystrophy Polymicrogyria Polyneuropathy Polyradiculoneuropathy Pseudoarylsulfatase a Deficiency Quadriplegia Refsum Disease, Classic Rem Sleep Behavior Disorder Renal Tubular Acidosis Retinitis Salivary Gland Adenoma, Pleomorphic Satb2-Associated Syndrome Schizophrenia Scott Syndrome Spasticity Spastic Paraparesis Spastic Paraplegia 13, Autosomal Dominant Spastic Paraplegia 2, X-Linked Spastic Quadriplegia Sphingolipidosis Spondylocarpotarsal Synostosis Syndrome Tay-Sachs Disease Thyroiditis Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Tremor Tubb4a-Related Leukodystrophy Undifferentiated Pleomorphic Sarcoma Van Der Woude Syndrome 1 Vasculitis Vasculopathy, Retinal, with Cerebral Leukodystrophy Wallerian Degeneration Xanthomatosis