DeCS

Descriptor en español:

Oftalmoplejía Externa Progresiva Crónica

Español de España

Descriptor	oftalmoplejía externa progresiva crónica
Término(s) alternativo(s)	CPEO OEPC distrofia muscular ocular enfermedad de Graefe miopatía mitocondrial ocular
Nota de alcance:	Miopatía mitocondrial caracterizada por parálisis lentamente progresiva de los músculos elevador del párpado, orbicular de los ojos, y musculatura extrínseca del ojo. En la biopsia muscular se encuentran fibras rojas rotas y atrofia. El inicio de la enfermedad suele ocurrir en la primera y segunda décadas de la vida, y la enfermedad progresa lentamente, hasta que, generalmente, se pierde la motilidad ocular. (Adams et al., Principles of Neurology, 6th ed, p1422)

Descriptor en inglés:

Ophthalmoplegia, Chronic Progressive External

Descriptor en portugués:

Oftalmoplegia Externa Progressiva Crônica

Descriptor en francés:

Ophtalmoplégie externe progressive

Término(s) alternativo(s):

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

Código(s) jeráquico(s):

C05.651.460.700
C10.292.562.750.250
C10.597.622.447.511
C10.668.491.500.700
C11.590.472.250
C18.452.660.560.700
C23.550.291.500.688
C23.888.592.636.447.511

Identificador Único RDF:

https://id.nlm.nih.gov/mesh/D017246

Nota de alcance:

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)

Nota de indización:

chronic progressive external ophthalmoplegia with cardiomyopathy & retinitis pigmentosa = KEARNS-SAYRE SYNDROME

Calificadores permitidos:

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

UI del concepto	M0026169
Nota de alcance	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)
Término preferido	Ophthalmoplegia, Chronic Progressive External
Término(s) alternativo(s)	CPEO Chronic Progressive External Ophthalmoplegia Disease, Graefe Dystrophy, Ocular Muscular External Ophthalmoplegia, Progressive Graefe Disease Graefe's Disease Mitochondrial Ocular Myopathy Muscular Dystrophies, Ocular Muscular Dystrophy, Ocular Myopathy, Mitochondrial Ocular Ocular Muscular Dystrophies Ocular Muscular Dystrophy Ocular Myopathy of Von Graefe Fuchs Ocular Myopathy of Von Graefe-Fuchs Ocular Myopathy, Mitochondrial Ophthalmoplegia, Progressive External Progressive External Ophthalmoplegia

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