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Amaurosis congenita of Leber, type III (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 3 is distinguished from the other forms of this condition by the genetic origin of the defect - chromosome 14q23.3, RDH12 gene.
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Amaurosis congenita of Leber, type 3:
»Introduction: Amaurosis congenita of Leber, type 3
»Symptoms of Amaurosis congenita of Leber, type 3
»Treatments for Amaurosis congenita of Leber, type 3
These medical condition or symptom topics may be relevant to medical information for Amaurosis congenita of Leber, type III:
Amaurosis congenita of Leber, type III: Another name for Amaurosis congenita of Leber, type 3 (or close medical condition association).
»Introduction: Amaurosis congenita of Leber, type 3
»Symptoms of Amaurosis congenita of Leber, type 3
»Treatments for Amaurosis congenita of Leber, type 3
Some of the symptoms of Amaurosis congenita of Leber, type III incude:
Treatments for Amaurosis congenita of Leber, type III (Amaurosis congenita of Leber, type 3) include:
Read more about treatments for Amaurosis congenita of Leber, type III
Treatment of Amaurosis congenita of Leber, type III: For more treatment information about Amaurosis congenita of Leber, type III, see treatment of Amaurosis congenita of Leber, type 3 (Amaurosis congenita of Leber, type III)
These medical disease topics may be related to Amaurosis congenita of Leber, type III:
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