STGD3 (medical condition): A rare genetic eye disorder that affects children and involves degeneration of the macula which is responsible for central vision which allows detailed visual function such as reading. Type 3 is caused by a defect in the ELOVL4 gene.
See also:
Stargardt disease 3:
»Introduction: Stargardt disease 3
»Symptoms of Stargardt disease 3
STGD3: Another name for Stargardt disease 3 (or close medical condition association).
»Introduction: Stargardt disease 3
»Symptoms of Stargardt disease 3
Some of the symptoms of STGD3 incude:
See full list of 6 symptoms of STGD3 (Stargardt disease 3)
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