Ophthalmoplegia, Chronic Progressive External [chronická progresivní externí oftalmoplegie]

topical
4
Terms

chronická progresivní externí ofthalmoplegie
CPEO
Graefeho nemoc
Graefova nemoc
oftalmoplegie chronická progresivní externí

 

Chronic Progressive External Ophthalmoplegia
CPEO
Graefe Disease
Graefe's Disease
Mitochondrial Ocular Myopathy
Ocular Muscular Dystrophy
Ocular Myopathy of Von Graefe-Fuchs
Ophthalmoplegia, Progressive External
Progressive External Ophthalmoplegia

Persistent link   https://www.medvik.cz/link/D017246
Definition

A mitochondrial myopathy characterized by slowly progressive paralysis of the levator palpebrae, orbicularis oculi, and extraocular muscles. Ragged-red fibers and atrophy are found on muscle biopsy. Familial and sporadic forms may occur. Disease onset is usually in the first or second decade of life, and the illness slowly progresses until usually all ocular motility is lost. (From Adams et al., Principles of Neurology, 6th ed, p1422)

Annotation
chronic progressive external ophthalmoplegia with cardiomyopathy & retinitis pigmentosa = KEARNS-SAYRE SYNDROME
DUI
D017246 MeSH Browser
CUI
M0026169
Previous indexing
DNA, Mitochondrial (1988-1992); Mitochondria, Muscle (1972-1992); Ophthalmoplegia (1966-1992)
History note
93
Public note
93

Allowable subheadings

BL
blood
CF
cerebrospinal fluid
CI
chemically induced
CL
classification 1
CO
complications
CN
congenital
DI
diagnosis 3
DG
diagnostic imaging
DH
diet therapy
DT
drug therapy
EC
economics
EM
embryology
EN
enzymology
EP
epidemiology
EH
ethnology
ET
etiology
GE
genetics 1
HI
history
IM
immunology
ME
metabolism
MI
microbiology
MO
mortality
NU
nursing
PS
parasitology
PA
pathology
PP
physiopathology 1
PC
prevention & control
PX
psychology
RT
radiotherapy
RH
rehabilitation
SU
surgery
TH
therapy
UR
urine
VE
veterinary
VI
virology

C Diseases
C05 Musculoskeletal Diseases 1 120
C05.651 Muscular Diseases 553
C05.651.460 Mitochondrial Myopathies 40
C05.651.460.620 Mitochondrial Encephalomyopathies 41
C05.651.460.700 Ophthalmoplegia, Chronic Progressive External 4
C05.651.460.700.500 Kearns-Sayre Syndrome 11
C10 Nervous System Diseases 1 878
C10.292 Cranial Nerve Diseases 60
C10.292.562 Ocular Motility Disorders 101
C10.292.562.750 Ophthalmoplegia 33
C10.292.562.750.250 Ophthalmoplegia, Chronic Progressive External 4
C10.292.562.750.250.500 Kearns-Sayre Syndrome 11
C10.292.562.750.375 Ophthalmoplegic Migraine 2
C10.292.562.750.500 Supranuclear Palsy, Progressive 50
C10.597 Neurologic Manifestations 1 052
C10.597.622 Paralysis 280
C10.597.622.447 Ophthalmoplegia 33
C10.597.622.447.511 Ophthalmoplegia, Chronic Progressive External 4
C10.597.622.447.511.500 Kearns-Sayre Syndrome 11
C10.597.622.447.600 Ophthalmoplegic Migraine 2
C10.597.622.447.690 Supranuclear Palsy, Progressive 50
C10.668 Neuromuscular Diseases 330
C10.668.491 Muscular Diseases 553
C10.668.491.500 Mitochondrial Myopathies 40
C10.668.491.500.500 Mitochondrial Encephalomyopathies 41
C10.668.491.500.700 Ophthalmoplegia, Chronic Progressive External 4
C10.668.491.500.700.500 Kearns-Sayre Syndrome 11
C11 Eye Diseases 1 489
C11.590 Ocular Motility Disorders 101
C11.590.472 Ophthalmoplegia 33
C11.590.472.250 Ophthalmoplegia, Chronic Progressive External 4
C11.590.472.250.500 Kearns-Sayre Syndrome 11
C11.590.472.375 Ophthalmoplegic Migraine 2
C11.590.472.500 Supranuclear Palsy, Progressive 50
C18 Nutritional and Metabolic Diseases 172
C18.452 Metabolic Diseases 1 196
C18.452.660 Mitochondrial Diseases 159
C18.452.660.560 Mitochondrial Myopathies 40
C18.452.660.560.620 Mitochondrial Encephalomyopathies 41
C18.452.660.560.700 Ophthalmoplegia, Chronic Progressive External 4
C18.452.660.560.700.500 Kearns-Sayre Syndrome 11
C23 Pathological Conditions, Signs and Symptoms 451
C23.550 Pathologic Processes 195
C23.550.291 Disease Attributes 1 208
C23.550.291.500 Chronic Disease 5 045
C23.550.291.500.063 Brain Damage, Chronic 253
C23.550.291.500.250 Candidiasis, Chronic Mucocutaneous 20
C23.550.291.500.266 Chemical and Drug Induced Liver Injury, Chronic 17
C23.550.291.500.282 Chronic Exertional Compartment Syndrome
C23.550.291.500.290 Chronic Kidney Disease-Mineral and Bone Disorder 146
C23.550.291.500.298 Chronic Limb-Threatening Ischemia 36
C23.550.291.500.313 Chronic Periodontitis 57
C23.550.291.500.360 Chronic Urticaria 17
C23.550.291.500.392 Fatigue Syndrome, Chronic 276
C23.550.291.500.423 Granulomatous Disease, Chronic 54
C23.550.291.500.431 Hematoma, Subdural, Chronic 25
C23.550.291.500.477 Hepatitis, Chronic 127
C23.550.291.500.479 Jaundice, Chronic Idiopathic 25
C23.550.291.500.483 Leukemia, Lymphocytic, Chronic, B-Cell 732
C23.550.291.500.485 Leukemia, Myelogenous, Chronic, BCR-ABL Positive 606
C23.550.291.500.493 Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative 15
C23.550.291.500.495 Leukemia, Myelomonocytic, Chronic 35
C23.550.291.500.497 Leukemia, Neutrophilic, Chronic 7
C23.550.291.500.500 Multiple Chronic Conditions 9
C23.550.291.500.625 Multiple Sclerosis, Chronic Progressive 155
C23.550.291.500.688 Ophthalmoplegia, Chronic Progressive External 4
C23.550.291.500.688.500 Kearns-Sayre Syndrome 11
C23.550.291.500.750 Pancreatitis, Chronic 230
C23.550.291.500.813 Polyradiculoneuropathy, Chronic Inflammatory Demyelinating 48
C23.550.291.500.829 Post-Infectious Disorders
C23.550.291.500.875 Pulmonary Disease, Chronic Obstructive 1 672
C23.550.291.500.906 Renal Insufficiency, Chronic 742
C23.550.291.500.937 Wasting Disease, Chronic 11
C23.888 Signs and Symptoms 3 919
C23.888.592 Neurologic Manifestations 1 052
C23.888.592.636 Paralysis 280
C23.888.592.636.447 Ophthalmoplegia 33
C23.888.592.636.447.511 Ophthalmoplegia, Chronic Progressive External 4
C23.888.592.636.447.511.500 Kearns-Sayre Syndrome 11
C23.888.592.636.447.600 Ophthalmoplegic Migraine 2
C23.888.592.636.447.690 Supranuclear Palsy, Progressive 50

Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 Disease MeSH Browser

Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 2 Disease MeSH Browser

Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 3 Disease MeSH Browser

Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 4 Disease MeSH Browser

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