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Iraqi Jewish optic atrophy plus (medical condition): A rare genetic condition where a gene mutation prevents the production of certain protein which leads to a build-up of an acid (3-methylglutaconic acid) which can have a negative impact on the body. The condition is characterized mainly by damage to the optic nerve.
See also:
3 alpha methylglutaconicaciduria, type 3:
»Introduction: 3 alpha methylglutaconicaciduria, type 3
»Symptoms of 3 alpha methylglutaconicaciduria, type 3
These medical condition or symptom topics may be relevant to medical information for Iraqi Jewish optic atrophy plus:
Iraqi Jewish optic atrophy plus is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Iraqi Jewish optic atrophy plus, or a subtype of Iraqi Jewish optic atrophy plus,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Iraqi Jewish optic atrophy plus: Another name for 3 alpha methylglutaconicaciduria, type 3 (or close medical condition association).
»Introduction: 3 alpha methylglutaconicaciduria, type 3
»Symptoms of 3 alpha methylglutaconicaciduria, type 3
Some of the symptoms of Iraqi Jewish optic atrophy plus incude:
These medical disease topics may be related to Iraqi Jewish optic atrophy plus:
Source - NIH
Search to find out more about Iraqi Jewish optic atrophy plus:
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