oftalmoplegie [Ophthalmoplegia]
- Termíny
-
oftalmoparéza
ophthalmoparesis
ophthalmoplegia
ophthalmoplegia externa
ophthalmoplegia interna
-
External Ophthalmoplegia
Internal Ophthalmoplegia
Oculomotor Paralysis
Ophthalmoparesis
Oftalmoplegie - ochrnutí očních svalů (vnitřních či zevních). (cit. Velký lékařský slovník online, 2013 http://lekarske.slovniky.cz/ )
Paralysis of one or more of the ocular muscles due to disorders of the eye muscles, neuromuscular junction, supporting soft tissue, tendons, or innervation to the muscles.
- Anotace
- do not confuse entry term OCULOMOTOR PARALYSIS with OCULOMOTOR NERVE PARALYSIS
- DUI
- D009886 MeSH Prohlížeč
- CUI
- M0015332
- Historická pozn.
- 1979; was OCULOMOTOR PARALYSIS 1963-1978
- Online pozn.
- use OPHTHALMOPLEGIA to search OCULOMOTOR PARALYSIS 1966-78
- Veřejná pozn.
- 1979; was OCULOMOTOR PARALYSIS 1963-1978
Povolená podhesla
- CI
- chemicky indukované
- SU
- chirurgie 2
- HI
- dějiny
- DG
- diagnostické zobrazování
- DI
- diagnóza 5
- DH
- dietoterapie
- EC
- ekonomika
- EM
- embryologie
- EN
- enzymologie
- EP
- epidemiologie 1
- ET
- etiologie 19
- EH
- etnologie
- DT
- farmakoterapie
- GE
- genetika 3
- IM
- imunologie
- CL
- klasifikace 2
- CO
- komplikace 2
- BL
- krev
- ME
- metabolismus
- MI
- mikrobiologie
- UR
- moč
- MO
- mortalita
- CF
- mozkomíšní mok
- NU
- ošetřování
- PS
- parazitologie
- PP
- patofyziologie 2
- PA
- patologie 2
- PC
- prevence a kontrola
- PX
- psychologie
- RT
- radioterapie
- RH
- rehabilitace 1
- TH
- terapie 2
- VE
- veterinární
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- virologie
- CN
- vrozené
CANOMAD syndrome Disease MeSH Prohlížeč
Fibrosis Of Extraocular Muscles, Congenital, 2 Disease MeSH Prohlížeč
Hamano Tsukamoto syndrome Disease MeSH Prohlížeč
Inclusion Body Myopathy 3, Autosomal Dominant Disease MeSH Prohlížeč
Inclusion body myopathy, autosomal dominant Disease MeSH Prohlížeč
Minicore Myopathy with External Ophthalmoplegia Disease MeSH Prohlížeč
Motor Neuron Disease with Dementia and Ophthalmoplegia Disease MeSH Prohlížeč
Ocular Myopathy with Curare Sensitivity Disease MeSH Prohlížeč
Oculomelic amyoplasia Disease MeSH Prohlížeč
Oculootoradial syndrome Disease MeSH Prohlížeč
Ophthalmoplegia Totalis with Ptosis and Miosis Disease MeSH Prohlížeč
Ophthalmoplegia, External, and Myopia Disease MeSH Prohlížeč
Ophthalmoplegia, Familial Static Disease MeSH Prohlížeč
Ophthalmoplegia, Familial Total, with Iris Transillumination Disease MeSH Prohlížeč
Ophthalmoplegia, Progressive, with Scrotal Tongue and Mental Deficiency Disease MeSH Prohlížeč
Ophthalmoplegic Neuromuscular Disorder with Abnormal Mitochondria Disease MeSH Prohlížeč
Optic Atrophy, Deafness, Ophthalmoplegia, and Myopathy Disease MeSH Prohlížeč
Progressive External Ophthalmoplegia With Hypogonadism Disease MeSH Prohlížeč
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1 Disease MeSH Prohlížeč
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Recessive Disease MeSH Prohlížeč
Schimke X-linked mental retardation syndrome Disease MeSH Prohlížeč
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis Disease MeSH Prohlížeč
Treft Sanborn Carey syndrome Disease MeSH Prohlížeč
Wieacker syndrome Disease MeSH Prohlížeč
congenital fibrosis of the extraocular muscles Disease MeSH Prohlížeč
external ophthalmoplegia, synergistic divergence, jaw winking, and oculocutaneous hypopigmentation Disease MeSH Prohlížeč