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Symptom Checker » Acute blindness » Eye symptoms
 

Acute blindness and Eye symptoms and Neovascular glaucoma in both eyes and Neovascular glaucoma in one eye
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Acute blindness and Eye symptoms and Neovascular glaucoma in both eyes and Neovascular glaucoma in one eye

  • Acute blindness AND Eye symptoms AND Neovascular glaucoma in both eyes AND Neovascular glaucoma in one eye - Causes of All Symptoms
  • Acute blindness OR Eye symptoms OR Neovascular glaucoma in both eyes OR Neovascular glaucoma in one eye - 5236 causes

Acute blindness:

Eye symptoms:

Neovascular glaucoma in both eyes:

Neovascular glaucoma in one eye:

Results: Causes of Acute blindness AND Eye symptoms AND Neovascular glaucoma in both eyes AND Neovascular glaucoma in one eye

    1. Eales Disease
     A rare eye disorder characterized by sudden vision loss, problems with eye blood vessuls and reoccurring eye blood vessel hemorrhages as well as oozing of clear thick fluid from inside the eyeball. Usually occurs after a stressful situation, trauma or aft...read more »

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Note: Do not use for diagnosis; see limitations of results.

Results: 5236 causes of Acute blindness OR Eye symptoms OR Neovascular glaucoma in both eyes OR Neovascular glaucoma in one eye

    1. 14q+ syndrome
     A rare chromosomal disorder involving duplication of genetic material from the long arm (q) of chromosome 14 resulting in various abnormalities....more »
    2. 14qter deletion Syndrome
     A very rare genetic condition where a portion at the end of the long arm (q) of chromosome 14 is missing....more »
    3. 18p minus syndrome
     A rare chromosomal disorder where a portion of chromosome 18 is missing which is characterized by mental and growth deficiencies, drooping upper eyelid and prominent ears. The type and severity of symptoms is determined by the amount of genetic material t...more »
    4. 1q deletion
     A rare chromosomal disorder where part of the long arm (q) of chromosome 1 is deleted resulting in various abnormalities which are determined by the size of the deleted portion....more »
    5. 1q terminal deletion
     A rare chromosomal disorder where the terminal part of the long arm (q) of chromosome 1 is deleted resulting in various abnormalities....more »
    6. 2-Hydroxyglutaricaciduria
     A rare metabolic disorder characterized by high levels of a certain chemical (2-Hydroxyglutaric) which causes a serious progressive neurological disease and damage to the brain. The features of this disorder are variable and some cases are milder than oth...more »
    7. 2-Methylbutyric Aciduria
     A very rare genetic disorder where an enzyme deficiency prevents the break down of certain proteins into energy and results in a harmful accumulation of acids in the blood and body tissues. More specifically, there is a deficiency of an enzyme (2-methylbu...more »
    8. 2-methylbutyryl-coenzyme A dehydrogenase deficiency
     A very rare genetic disorder where an enzyme deficiency prevents the break down of certain proteins into energy and results in a harmful accumulation of acids in the blood and body tissues. More specifically, there is a deficiency of an enzyme (2-methylbu...more »
    9. 22q11.2 deletion syndrome
     A rare genetic disorder caused by the absence of a small portion of genetic material. A small section of chromosome 22 is missing at a location called q11.2. Chromosome 22 is one of 23 pairs of chromosomes that exist in humans....more »
    10. 2p21 deletion syndrome
     This syndrome is a more severe form hypotonia-cystinuria syndrome as a larger portion of genetic material from chromosome 2p21 is deleted. It is characterized by infant seizures, reduced muscle tone, developmental delay, lactic acidosis and unusual facial...more »

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  • Warning - Beta version - information may be incorrect (details)
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