Informaţii despre

Nume Kearns-Sayre Syndrome
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli metabolice; Boli rare
Clasificari ICD10 Other paralytic strabismus; Total (external) ophthalmoplegia
Clasificare anatomică Malacards Boli ale ochiului; Boli ale urechii; Boli cardiovasculare; Boli endocrine; Boli musculare; Boli neuronale

Vezi şi

Boli A-Z 3-Methylglutaconic Aciduria, Type V Aceruloplasminemia 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 Alport Syndrome, X-Linked Al-Raqad Syndrome Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Ataxia-Oculomotor Apraxia 3 Atrial Standstill 1 Atrioventricular Block Autosomal Dominant Progressive External Ophthalmoplegia Axonal Neuropathy Basal Ganglia Calcification Blood Group--Ahonen Blood Group, I System Cardiac Arrest Cardiac Conduction Defect Cardiogenic Shock Cardiomyopathy, Familial Hypertrophic, 1 Cardiomyopathy, Infantile Hypertrophic Carney Triad Cerebellar Disease Cerebral Folate Deficiency Cerebritis Cervicitis Choroideremia Choroiditis Chronic Progressive External Ophthalmoplegia Congestive Heart Failure Corneal Dystrophy Cortical Blindness Cowden Syndrome 3 Cranial Nerve Disease Diabetes and Deafness, Maternally Inherited Diabetes Mellitus Dilated Cardiomyopathy Diphyllobothriasis Dysphagia Dystonia Early Myoclonic Encephalopathy Encephalomyopathy Encephalopathy Endotheliitis Exotropia Facial Nerve Disease Fanconi Syndrome Fibrosis of Extraocular Muscles, Congenital, 2 Gout Growth Hormone Deficiency Hereditary Ataxia Hyperglycemia Hypersomnia Hypomelanosis of Ito Hypoparathyroidism Hypopituitarism Hypotropia Intestinal Pseudo-Obstruction Isolated Atp Synthase Deficiency Lactic Acidosis Leber Hereditary Optic Neuropathy Leber Optic Atrophy Leber Optic Atrophy and Dystonia Leigh Syndrome Leukodystrophy Long Qt Syndrome Macular Dystrophy, Vitelliform, 3 Metabolic Acidosis Mitochondrial Complex Ii Deficiency Mitochondrial Complex Iv Deficiency Mitochondrial Complex V Deficiency Mitochondrial Disorders Mitochondrial Dna-Associated Leigh Syndrome and Narp Mitochondrial Dna Depletion Syndrome 1 Mitochondrial Dna Depletion Syndrome 4a Mitochondrial Dna Depletion Syndrome 7 Mitochondrial Encephalomyopathy Mitochondrial Metabolism Disease Mitochondrial Myopathy Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes Mitochondrial Neurogastrointestinal Encephalomyopathy Mitochondrial Neurogastrointestinal Encephalopathy Disease Moebius Syndrome Mungan Syndrome Myoclonic Epilepsy Associated with Ragged-Red Fibers Myopathy Myopathy, Lactic Acidosis, and Sideroblastic Anemia Neural Crest Tumor Neuritis Neuromuscular Disease Neuropathy Ocular Motility Disease Ocular Motor Apraxia Open-Angle Glaucoma Optic Nerve Disease Optic Neuritis Pancreatitis Paraganglioma and Gastric Stromal Sarcoma Paragangliomas 1 Paralytic Ileus Paralytic Squint Parkinson Disease 6, Autosomal Recessive Early-Onset Pearson Marrow-Pancreas Syndrome Periodic Paralysis with Later-Onset Distal Motor Neuropathy Peripheral Nervous System Disease Polyneuropathy Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 3 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Recessive 1 Progressive Familial Heart Block, Type Ib Ptosis Pyle Disease Radiculopathy Renal Tubular Acidosis Retinitis Sensorineural Hearing Loss Sensory Ataxic Neuropathy, Dysarthria, and Ophthalmoparesis Sideroblastic Anemia Somatoform Disorder Sparganosis Spastic Ataxia Spastic Ataxia, Charlevoix-Saguenay Type Spastic Quadriplegia Strabismus Syncope Thyroiditis Tukel Syndrome Vitelliform Macular Dystrophy