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Amaurosis congenita of Leber, type XI (medical condition): A rare inherited retinal disease (retinal dystrophy) that starts during the fetal stage. Vision impairment is obvious at birth or within months of birth. Type 11 is distinguished from the other forms of this condition by the genetic origin of the defect - chromosome 7q, IMPDH1 gene.
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Amaurosis congenita of Leber, type 11:
»Introduction: Amaurosis congenita of Leber, type 11
»Symptoms of Amaurosis congenita of Leber, type 11
These medical condition or symptom topics may be relevant to medical information for Amaurosis congenita of Leber, type XI:
Amaurosis congenita of Leber, type XI: Another name for Amaurosis congenita of Leber, type 11 (or close medical condition association).
»Introduction: Amaurosis congenita of Leber, type 11
»Symptoms of Amaurosis congenita of Leber, type 11
Some of the symptoms of Amaurosis congenita of Leber, type XI incude:
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