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视神经萎缩(Optic atrophy)
视神经萎缩(Optic atrophy)
Optic nerve atrophy can be caused by a variety of reasons, common ischemia, inflammation, compression, trauma and demyelinating diseases, as follows:
1. secondary optic atrophy secondary to intracranial hypertension
2. intracranial inflammation, more common in tuberculous meningitis or optic disc inflammation
3. retinopathy
The vascular and central retinal artery or vein occlusion, optic nerve itself arteriosclerosis, vascular disorders, normal nutrition hemorrhage (digestive tract and uterus)
The inflammation
The [1] after glaucoma.
The retinal pigment degeneration
The Refsum disease
Melano.
4. optic neuritis and optic neuropathy
The blood vessels, such as ischemic optic neuropathy
The demyelinating disease
The lack of vitamin
Because the lead or other metal poisoning
The herpes zoster
Syphilitic.
5. compression induced
The tumors include meningioma, craniopharyngioma, pituitary adenoma, and aneurysm (anterior communicating artery aneurysm)
Bone diseases, including Paget disease, osteitis deformans, skull stenosis disease
Orbital tumor
6. trauma
7. metabolic diseases, such as diabetes mellitus, gangliosides, etc.
8. hereditary diseases
Lebers disease, cerebellar ataxia, peripheral neuropathy, such as Chareot-Marie-Tooths disease
9. trophic optic atrophy
10. miscellaneous
In children, the reasons are more complex as follows:
1. chromosome abnormality
Criduchat syndrome, deletion of the long arm of chromosome 18
2. fat disease
Tay-sachss disease, Sandhoffss disease, lactose (nerve), sphingosine poisoning, NIEMANN-Piecks disease, alpha beta lipoprotein (Bassen-kornzwig syndrome)
3., mucopolysaccharide
Hurlers mucopolysaccharide disease, with cystine disease
4. mineral metabolism defects and their metabolism
Menkess disease, juvenile diabetes mellitus, cystic fibrosis of the pancreas, Albers-Schouml, Zellwages disease, and nbergs disease
5. hereditary pigmentary degeneration of the retina
Ushers syndrome, Kesrns-Sayer syndrome, Alstrom syndrome
6.
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